U.S. patent application number 15/702529 was filed with the patent office on 2018-05-03 for n-acetyl mannosammine as a therapeutic agent.
This patent application is currently assigned to The United States of America, as represented by the Secretary, Department of Health and Human. The applicant listed for this patent is The United States of America, as represented by the Secretary, Department of Health and Human, The United States of America, as represented by the Secretary, Department of Health and Human. Invention is credited to William A. Gahl, Marjan Huizing, Enriko Klootwijk, Irini Manoli.
Application Number | 20180117072 15/702529 |
Document ID | / |
Family ID | 39952249 |
Filed Date | 2018-05-03 |
United States Patent
Application |
20180117072 |
Kind Code |
A1 |
Huizing; Marjan ; et
al. |
May 3, 2018 |
N-ACETYL MANNOSAMMINE AS A THERAPEUTIC AGENT
Abstract
The invention relates to compositions and methods for treating
kidney and muscle dysfunction that involves use of therapeutic
amounts of N-acetyl mannosamine.
Inventors: |
Huizing; Marjan; (Santa
Cruz, CA) ; Gahl; William A.; (Kensington, MD)
; Manoli; Irini; (Rockville, MD) ; Klootwijk;
Enriko; (London, GB) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
The United States of America, as represented by the Secretary,
Department of Health and Human |
Bethesda |
MD |
US |
|
|
Assignee: |
The United States of America, as
represented by the Secretary, Department of Health and
Human
Bethesda
MD
|
Family ID: |
39952249 |
Appl. No.: |
15/702529 |
Filed: |
September 12, 2017 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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14754304 |
Jun 29, 2015 |
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15702529 |
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13791576 |
Mar 8, 2013 |
9095597 |
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14754304 |
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12530433 |
Mar 19, 2010 |
8410063 |
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PCT/US2008/006895 |
May 30, 2008 |
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13791576 |
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60932451 |
May 31, 2007 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61P 13/12 20180101;
A61P 21/04 20180101; A61K 31/7012 20130101; A61P 21/00 20180101;
A61K 31/7008 20130101; A61P 43/00 20180101 |
International
Class: |
A61K 31/7008 20060101
A61K031/7008; A61K 31/7012 20060101 A61K031/7012 |
Goverment Interests
GOVERNMENT FUNDING
[0002] The invention described herein was developed with support
from the National Human Genome Research Institute (NHGRI), which is
part of the National Institutes of Health (NIH). The United States
Government has certain rights in the invention.
Claims
1. A method of treating a condition or disease in a mammal in need
thereof comprising administering an effective amount of a sialic
acid precursor, N-acetyl mannosamine or a derivative thereof, to
the mammal, wherein the derivative consists of Formula I.
##STR00003## wherein R.sub.1, R.sub.3, R.sub.4, or R.sub.5 is
hydrogen, lower alkanoyl, carboxylate or lower alkyl; R.sub.2 is
lower alkyl, lower alkanoylalkyl, lower alkyl alkanoyloxy; and the
condition or disease is selected from muscular atrophy, muscular
dystrophy, high blood pressure, or diabetes.
2. The method of claim 1, comprising administering a therapeutic
amount of N-acetyl mannosamine to the mammal.
3. The method of claim 2, wherein the therapeutic amount is about
0.1 g to about 50 g N-acetyl mannosamine per day.
4. The method of claim 2, wherein the therapeutic amount is
administered in a unit dosage of about 0.01 g to about 50 g
N-acetyl mannosamine per unit dosage.
5. The method of claim 1, comprising sustained release of the
sialic acid precursor, N-acetyl mannosamine or a derivative
thereof.
6. The method of claim 1, comprising topical administration of the
sialic acid precursor, N-acetyl mannosamine or a derivative
thereof.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 14/754,304, filed Jun. 29, 2015, which is a
continuation of U.S. patent application Ser. No. 13/791,576, filed
Mar. 8, 2013, and issued as U.S. Pat. No. 9,085,597 on Aug. 4,
2015, which is a continuation of U.S. patent application Ser. No.
12/530,433, filed Mar. 19, 2010, and issued as U.S. Pat. No.
8,410,063 on Apr. 2, 2013, which is the U.S. National Stage of
International Application No. PCT/US2008/006895, filed May 30,
2008, which was published in English under PCT Article 21(2), which
in turn claims the benefit of U.S. Provisional Patent Application
No. 60/932,451, filed May 31, 2007, all of which are hereby
incorporated by reference.
FIELD OF THE INVENTION
[0003] The invention is related to a methods and compositions
involving use of the neutral sugar N-acetyl mannosamine (ManNAc)
for therapeutic purposes in humans. Such therapeutic uses include
treatment of myopathies (e.g., hereditary inclusion body myopathy
(HIBM)) and certain kidney diseases (e.g., those involving
proteinuria and hematuria).
BACKGROUND OF THE INVENTION
[0004] Hereditary inclusion body myopathy (HIBM; OMIM 600737) is a
rare autosomal recessive neuromuscular disorder. Argov, et al.,
Neurology 60, 1519-1523 (2003); Eisenberg, et al. (2001) Nat Genet
29, 83-87 (2001); Griggs, et al. (1995) Ann Neurol 38, 705-713
(1995). The disease usually manifests at approximately 20 years of
age with foot drop and slowly progressive muscle weakness and
atrophy. Histologically, it is associated with muscle fiber
degeneration and formation of vacuoles containing 15-18 nm
tubulofilaments that immunoreact like .beta.-amyloid, ubiquitin,
prion protein and other amyloid-related proteins. Askanas et al.
Curr Opin Rheumatol 10, 530-542 (1998); Nishino, et al. (2005) Acta
Myol 24, 80-83 (2005); Askanas, et al. Ann Neurol 34, 551-560
(1993); Argov, et al. Curr Opin Rheumatol 10, 543-547 (1998). Both
weakness and histological changes initially spare the quadriceps.
However, the disease is relentlessly progressive, with patients
becoming incapacitated and wheelchair-confined within two to three
decades. There is no treatment available.
[0005] Accordingly, new compositions and methods are needed for
treating hereditary inclusion body myopathy and related
diseases.
SUMMARY OF THE INVENTION
[0006] One aspect of the invention is a therapeutic method for
increasing sialic acid in a mammal in need thereof comprising
administering to the mammal an effective amount of N-acetyl
mannosamine or a derivative thereof to thereby increase sialic acid
in the mammal.
[0007] In some embodiments, such methods are performed to treat a
disease or condition. For example, such a disease can be muscular
atrophy or kidney disease. In general, the types of muscular
atrophies that can be treated by the methods and compositions of
the invention are those caused by sialic acid deficiency. Examples
of such muscular atrophy diseases and conditions include distal
myopathy with rimmed vacuoles (Nonaka myopathy) and hereditary
inclusion body myopathy.
[0008] Surprisingly, the compositions and methods of the invention
are useful for treating certain kidney conditions and diseases, for
example, those involving proteinuria, hematuria resulting primarily
or secondarily from hyposialylation (lack of sialic acid). Thus,
the present methods are effective for treatment of kidney disorders
due to poor kidney membrane formation and/or function. For example,
kidney membranes that are affected by loss of sialic acid include
the glomerular basement membrane and/or the podocyte membranes.
Hence, the invention is useful for treating malformed or poorly
functioning glomerular basement membranes and/or podocyte
membranes. In general, the methods of the invention can increase
sialylation of kidney podocalyxin, improve podocyte foot process
morphology and/or improve glomerular basement membrane
integrity.
[0009] Another aspect of the invention is a method of treating a
kidney disorder in a mammal comprising administering a therapeutic
amount of N-acetyl mannosamine or a derivative thereof to the
mammal, wherein the kidney disorder involves proteinuria and
hematuria. For example, such a therapeutic amount of N-acetyl
mannosamine or a derivative thereof is about 1 g to about 20 g per
day.
DESCRIPTION OF THE FIGURES
[0010] FIG. 1 schematically illustrates the intracellular
metabolism of sialic acid. This figure shows portions of a cell,
where the nucleus is depicted at the bottom (below the depicted
nuclear membrane) and the cytoplasm is at the top of the figure.
Cytosolic glucose is converted in several steps into UDP-GlcNAc,
which serves as substrate for the bi-functional, rate-limiting,
committed enzyme for sialic acid biosynthesis: UDP-GlcNAc
2-epimerase/ManNAc kinase (GNE/MNK). GNE catalytic activity (EC
5.1.3.14) epimerizes UDP-GlcNAc to ManNAc, followed by the
phosphorylation of ManNAc to ManNAc-6-phosphate (MaNAc-6-P) by the
MNK kinase catalytic domain (EC 2.7.1.60). ManNAc-6-phosphate is
then condensed with phosphoenolpyruvate to Neu5Ac-9-phosphate by
Neu5Ac-9-P synthetase. The phosphate is then released and Neu5Ac is
activated by CMP-Neu5Ac synthetase to CMP-Neu5Ac in the nucleus.
CMP-Neu5Ac then enters the trans-Golgi and serves as the substrate
for different sialyltransferases involved in the production of
sialylated glycoconjugates. These are subsequently cleaved in the
lysosome to yield free sialic acid, which is exported to the
cytoplasm and re-utilized or degraded to ManNAc and pyruvate.
CMP-sialic acid strongly feedback inhibits the GNE epimerase at its
allosteric site.
[0011] FIG. 2A-E illustrates the generation and identification of
GneM712T/M712T knockin mice. FIG. 2A is a schematic diagram
illustrating the murine Gne (Ueal) genomic locus, exons 11 and 12,
after homologous recombination with the sequence-verified targeting
vector. The M712T mutation was created in exon 12, and a neo
cassette (under the PGK promoter) flanked by flippase recombinase
target (FRT) sites was inserted. LoxP sites were inserted before
exon 12 and after the PGK-neo gene. FIG. 2B shows the genotyping of
mutant mice. A PCR-amplified 387-bp fragment of genomic DNA across
the M712T (ATG to ACG) mutation was digested by the NlaIII
restriction endonuclease into 265-bp, 89-bp, and 33-bp fragments in
a wild-type allele (+) and into 354-bp and 33-bp fragments in a
mutant M712T allele (-). MW, molecular weight. FIG. 2C shows the
results of RT-PCR of kidney and skeletal muscle RNA. RNA was
reverse transcribed and PCR-amplified using primers covering exons
11 and 12 (355 bp). Digestion by NlaIII cut the wild-type allele
(+) into 225-bp, 89-bp, and 41-bp fragments and the mutant M712T
allele (-) into 314-bp and 41-bp fragments. Digestion confirmed the
exclusive presence of the mutant M712T allele in
Gne.sup.M712T/M712T (-/-) tissues. FIG. 2D shows the numbers and
genotypes of mice at E17-E19 and P21. At P21, genotyping of 76 mice
from 13 litters (9 Gne.sup.M712T/+ matings) identified only 1
Gne.sup.M712T/M712T offspring. Subsequent genotyping of 35 E17-E19
embryos from 4 Gne.sup.M712T/+ mice yielded a Mendelian
distribution of genotypes. FIG. 2E shows that at P2,
Gne.sup.M712T/M712T pups were smaller than their heterozygous
(Gne.sup.M712T/+) and wild-type (Gne.sup.+/+) littermates and
lacked a prominent milkspot.
[0012] FIG. 3A-E provides results of histological kidney analyses.
FIG. 3A illustrates gross kidney pathology. Kidneys of
Gne.sup.M712T/M712T mice showed hemorrhages but were normal in size
and shape compared with kidneys of wild-type (Gne.sup.+/+) and
heterozygous (Gne.sup.M712T/+) littermates. FIG. 3B shows
representative H&E-stained sections of renal cortex (c) and
medulla (m) showing tubular dilatations in Gne.sup.M712T/M712T mice
(arrows). Scale bars: 1,000 .mu.m. FIG. 3C provides high
magnification images of collecting ducts, renal tubules, and
urinary space, filled with red blood cells in Gne.sup.M712T/M712T
mice. Scale bars: 100 .mu.m. FIG. 3D provides high magnification
images of glomeruli (g) with red blood cells infiltrated into the
Bowman space in Gne.sup.M712T/M712T mice. Scale bars: 100 .mu.m
FIG. 3E shows representative sections of normal glomerulus (DICII,
left panel) demonstrating the abundance of Gne/Mnk protein inside
the glomerular space upon immunolabeling with Gne/Mnk antibodies
(FITC filter, right panel). Scale bars: 50 .mu.m.
[0013] FIG. 4A-D shows transmission electron microscope images of
mouse kidney sections. FIG. 4A shows representative cross-sections
of glomerular capillaries in the juxtamedullar zone of a wild-type
mouse (age P2). Enlarged insets (right panels) show detailed
endothelial cells (ec), glomerular basement membrane (GBM);
arrowheads), and foot processes (fp) of the glomerular epithelial
cells (podocytes) with well formed, open filtration slits
(asterisks). FIG. 4B shows representative juxtamedullary glomerular
capillaries of a Gne.sup.M712T/M712T mouse (age P2, littermate of
the wild-type mouse shown in FIG. 4A), indicating segmental
splitting of the lamina densa of the GBM (arrowheads) as well as
dramatically flattened and fused podocyte foot processes lining the
GBM. The filtration slits are sparse and irregular in shape and
position. Insets (right panels) show fused foot process membranes
and formation of abnormal tight junction-like structures at the
filtration slits (diamonds). FIGS. 4C and 4D representative
glomerular capillaries of a Gne.sup.M712T/M712T mouse following
ManNAc treatment (age P19). The integrity of the GBM as well as the
formation of podocyte foot processes and the number of filtration
slits were all improved when compared with the untreated
Gne.sup.M712T/M712T mouse in FIG. 4B. Some filtration slits were
open, while others still formed tight junctions. The GMB showed
occasional small stretches of areas where splitting was apparent
(arrowheads). L, capillary lumen; N, nucleus; us, urinary space.
Scale bars: 1 .mu.m.
[0014] FIG. 5A-5F illustrates the biochemistry and renal histology
of knockin mice following ManNAc treatment. FIG. 5A shows the
numbers of mice surviving past age P3 after ManNAc administration
in the drinking water of Gne.sup.M712T/+ mice. Six Gne.sup.M712T/+
mice received 1 mg/ml (.about.0.2 g/kg/d) ManNAc; 7 total litters
were scored; 13 pups died at age P1-P3. Seven Gne.sup.M712T/+ mice
received 5 mg/ml (.about.1 g/kg/d) ManNAc; 13 total litters were
scored; 14 homozygous mutant pups died at age P1-P3. The percentage
of survivors of each genotype is indicated. FIG. 5B-5D shows
representative H&E-stained kidney sections showing renal cortex
and medulla (FIG. 5B); collecting ducts, renal tubules, and urinary
space (FIG. 5C); and glomeruli (FIG. 5D) following ManNAc feeding
at age P6. Wild-type (Gne+/+) kidneys showed normal histology.
Gne.sup.M712T/M712T kidneys showed a range from very mild (middle
panel) to moderately severe (right panel) red blood cell
infiltrations, but in all cases less severe than in untreated
Gne.sup.M712T/M712T mice at age P2 (FIG. 5E-G). Scale bars: 500
.mu.m (FIG. 5B), 100 mm (FIGS. 5C and 5D). FIG. 5E shows two
ManNAc-treated (.about.1 g/kg/d) 6-week-old male littermates.
Surviving homozygous mutant mice (Gne.sup.M712T/M712T) were smaller
than their wild-type littermates. FIG. 5F shows Gne/Mnk epimerase
enzymatic activities in skeletal muscle. Administration of ManNAc
(shaded bars) increased the activity in wild-type muscle from 100%
to 114% (.+-.19.7) (n=3; P=0.2) and increased the activity in
homozygous mutant (Gne.sup.M712T/M712T ) muscle from 19.4%
(.+-.7.5) to 31% (.+-.8.4) (n=7; P=0.05).
[0015] FIG. 6A-E shows immunoblots of muscle, kidney, and brain
extracts of knockin mice. Immunoblots of muscle (FIG. 6A) and
kidney (FIG. 6B) extracts exhibited decreased Gne/Mnk protein
expression (upper band, arrows, 79 kDa) in homozygous mutant
Gne.sup.M712T/M712T (-/-) mice compared with heterozygous (+/-) and
wild-type (+/+) littermates (normalized to .beta.-actin). Gne/Mnk
protein expression increased upon ManNAc feeding in
Gne.sup.M712T/M712T (-/-) tissues when compared with untreated
tissues. FIG. 6C shows immunoblots of kidney extracts labeled with
laminin-1 antibodies. No difference in laminin-1 intensity was
detected (n=6; P=0.65) between Gne.sup.+/+ (+/+) and
Gne.sup.M712T/M712T (-/-) littermates without or with ManNAc
treatment. FIG. 6D shows representative immunoblots of brain
extracts labeled with PSA-NCAM antibodies. Upon ManNAc treatment,
the intensity of the PSA-NCAM signals, reflecting sialylation
status, increased by 2% to 28% in treated Gne.sup.M712T/M712T (-/-)
brain (n=14) when compared with untreated brain (n=10). FIG. 6E
shows immunoblots of kidney extracts (age P2) labeled with
antibodies against podocalyxin (.about.140-150 kDa). Top: Following
desialylation of Gne.sup.+/+ (+/+), Gne.sup.M712T/+ (+/-), or
Gne.sup.M712T/M712T (-/-) kidney extracts by neuraminidase (lanes 2
and 4), podocalyxin migrated more slowly (.about.160-180 kDa) than
untreated samples (lanes 1 and 3). Gne.sup.M712T/M712T (-/-) kidney
extracts (lanes 5 and 6) contained desialylated podocalyxin.
Bottom: Sialylation of podocalyxin at P6 in Gne.sup.M712T/M712T
(-/-) mice changed significantly after ManNAc treatment (lanes 3
and 4).
[0016] FIG. 7 schematically illustrates a timeline for
administration of N-acetyl mannosamine during a clinical trial of
human patients.
DETAILED DESCRIPTION OF THE INVENTION
[0017] According to the invention, N-acetyl-mannosamine and
derivatives thereof are useful for treating a variety of diseases
and conditions. N-acetyl-D-mannosamine is a key compound in the
sialic acid biosynthetic pathway (see FIG. 1). In particular, there
is a regulated, rate-limiting enzymatic step in the pathway that
leads to sialic acid formation, and this rate-limiting step gives
rise to N-acetyl-D-mannosamine. Hence, once N-acetyl-D-mannosamine
is formed or administered, no other enzymatic step leading to the
formation of sialic acid is subject to feedback inhibition. Thus,
administration of N-acetyl-D-mannosamine will lead to increased
amounts of sialic acid. The structure of N-acetyl-mannosamine is
shown below.
##STR00001##
[0018] Therefore, according to the invention, administration of
N-acetyl mannosamine (ManNAc) and/or its derivatives promotes
formation of sialic acid (N-acetylneuramic acid). Sialic acids are
sugars found on many cellular and tissue components. For example,
sialic acids are present on most cell surfaces, and on proteins and
lipids and are involved in cell to cell interactions. Sialic
acid-rich oligosaccharides on the glycoconjugates found on surface
membranes help keep water at the surface of cells. The sialic
acid-rich regions also contribute to creating a negative charge on
the cells surface. Since water is a polar molecule, it is attracted
to cell surfaces and membranes. Thus, sialic acids contribute to
cellular hydration and fluid uptake. Sialic acid is also a vital
component of many body fluids including, serum, cerebrospinal,
saliva, amniotic, and mother's milk.
N-Acetylmannosamine Derivatives
[0019] According to the invention, N-acetylmannosamine and
derivatives thereof can also be used in the therapeutic methods and
compositions of the invention. The structures of such
N-acetylmannosamine derivatives useful in the invention are defined
by Formula I.
##STR00002##
wherein:
[0020] R.sub.1, R.sub.3, R.sub.4, or R.sub.5 is hydrogen, lower
alkanoyl, carboxylate or lower alkyl; and
[0021] R.sub.2 is lower alkyl, lower alkanoylalkyl, lower alkyl
alkanoyloxy.
[0022] The following definitions are used, unless otherwise
described: Alkyl, alkoxy, alkenyl, alkynyl, etc. denote both
straight and branched groups; but reference to an individual
radical such as "propyl" embraces only the straight chain radical,
a branched chain isomer such as "isopropyl" being specifically
referred to.
[0023] Lower alkyl refers to (C.sub.1-C.sub.6)alkyl. Such a lower
alkyl or (C.sub.1-C.sub.6)alkyl can be methyl, ethyl, propyl,
isopropyl, butyl, iso-butyl, sec-butyl, pentyl, 3-pentyl, or hexyl;
(C.sub.3-C.sub.6)cycloalkyl can be cyclopropyl, cyclobutyl,
cyclopentyl, or cyclohexyl;
(C.sub.3-C.sub.6)cycloalkyl(C.sub.1-C.sub.6)alkyl can be
cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl,
cyclohexylmethyl, 2-cyclopropylethyl, 2-cyclobutylethyl,
2-cyclopentylethyl, or 2-cyclohexylethyl; (C.sub.1-C.sub.6)alkoxy
can be methoxy, ethoxy, propoxy, isopropoxy, butoxy, iso-butoxy,
sec-butoxy, pentoxy, 3-pentoxy, or hexyloxy;
(C.sub.2-C.sub.6)alkenyl can be vinyl, allyl, 1-propenyl,
2-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1,-pentenyl,
2-pentenyl, 3-pentenyl, 4-pentenyl, 1- hexenyl, 2-hexenyl,
3-hexenyl, 4-hexenyl, or 5-hexenyl; (C.sub.2-C.sub.6)alkynyl can be
ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl,
1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1- hexynyl,
2-hexynyl, 3-hexynyl, 4-hexynyl, or 5-hexynyl;
(C.sub.1-C.sub.6)alkanoyl can be acetyl, propanoyl or butanoyl;
halo(C.sub.1-C.sub.6)alkyl can be iodomethyl, bromomethyl,
chloromethyl, fluoromethyl, trifluoromethyl, 2-chloroethyl,
2-fluoroethyl, 2,2,2-trifluoroethyl, or pentafluoroethyl;
hydroxy(C.sub.1-C.sub.6)alkyl can be hydroxymethyl, 1-hydroxyethyl,
2-hydroxyethyl, 1-hydroxypropyl, 2-hydroxypropyl, 3-hydroxypropyl,
1-hydroxybutyl, 4-hydroxybutyl, 1-hydroxypentyl, 5-hydroxypentyl,
1-hydroxyhexyl, or 6-hydroxyhexyl; (C.sub.1-C.sub.6)alkoxycarbonyl
can be methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl,
isopropoxycarbonyl, butoxycarbonyl, pentoxycarbonyl, or
hexyloxycarbonyl; (C.sub.1-C.sub.6)alkylthio can be methylthio,
ethylthio, propylthio, isopropylthio, butylthio, isobutylthio,
pentylthio, or hexylthio; (C.sub.2-C.sub.6)alkanoyloxy can be
acetoxy, propanoyloxy, butanoyloxy, isobutanoyloxy, pentanoyloxy,
or hexanoyloxy.
Therapeutic Methods
[0024] According to the invention, N-acetyl-D-mannosamine (ManNAc)
and derivatives thereof are useful therapeutic agents for
increasing production of sialic acids in mammals, and such
increased production of sialic acid has profound therapeutic
benefits. Sialic acids are important for proper development and
functioning of many organs and tissues, and a deficiency of sialic
acid can give rise to many different types of diseases and
conditions. For example, abnormalities of sialic acid metabolism
cause a severe infantile disease (infantile sialic acid storage
disease, ISSD), characterized by failure to thrive,
hepatosplenomegaly, coarse facial features, severe mental and motor
retardation presenting at birth and often leading to death within
the first year of life, or diseases of later onset (Salla disease,
sialuria).
[0025] As shown herein, administration of ManNAc (and derivatives
thereof) is useful for treating myopathies, muscular atrophy and/or
muscular dystrophy (e.g., hereditary inclusion body myopathy
(HIBM)) and kidney conditions and diseases (e.g., those involving
proteinuria and hematuria).
[0026] Myopathies that can be treated with the present compositions
and methods also include distal myopathy with rimmed vacuoles
(Nonaka myopathy) and the muscular dystrophy hereditary inclusion
body myopathy (HIBM).
[0027] Proteinuria involves leakage of protein from the blood into
the urine. If the amount of protein in the urine is very high, this
condition is often called nephrotic syndrome. While there may be
many causes for nephritic syndrome, according to the invention at
least one cause is a deficiency of sialic acid, which has a direct
impact on the formation, structure and function of kidney glomeruli
and the membranes associated therewith. Several types of diseases
exhibit the symptoms of proteinuria, including high blood pressure,
infections, reflux nephropathy, diabetes, various types of
glomerulonephritis, including minimal change nephrosis. However, by
improving the structure and function of nephron components that
require sialic acid, the present compositions and methods can treat
any of these diseases. Thus, for example, the methods and
compositions of the invention dramatically improve kidney function
by improving the structure and filtration properties of kidneys,
thereby reducing the amount of protein in the urine and/or the
severity or progression of proteinuria.
[0028] Hematuria simply means blood in the urine. The blood may be
visible, so that the urine appears reddish or darker than normal
(called gross hematuria). If the blood is invisible and is
discovered only when a urine sample is examined in a laboratory
urine test, the condition is called microscopic hematuria. In
general, hematuria is more a symptom than a condition in itself,
because it has many possible causes. A urinary tract infection,
kidney or bladder stones, an enlarged prostate in men, cystitis (a
bladder infection, usually in women) or bladder, kidney or prostate
cancer can all cause hematuria. Other causes include injuries that
result in a bruised kidneys; sickle cell anemia and other abnormal
red blood cell diseases; and certain medications, such as blood
thinners (e.g., aspirin and some other pain relief medicines). More
specific causes of glomerular basal membrane dysfunction, such as
Alport disease, thin membrane disease, and IgA nephropathy, may
particularly improve when the treatment methods described herein
are employed.
[0029] In general, the treatment methods of the invention involve
administering to a mammal (or patient) a therapeutically effective
amount of N-acetyl mannosamine and/or a derivative thereof. Such a
therapeutically effective amount is generally given daily for
appropriate periods of time. Effective amounts for human patients
are, for example, about 0.1 g/day to about 50 g/day, of about 0.2
g/day to about 25 g/day, from about 0.3 g/day to about 12 g/day,
from about 0.4 g/day to about 10 g/day, from about 0.5 g/day to
about 8 g/day, and from about 0.7 g/day to about 6 g/day.
Generally, N-acetyl mannosamine and/or a derivative thereof is
administered for periods of time sufficient to increase the amount
of sialic acid in the mammal and thereby achieve a therapeutic
benefit. Therapeutic benefits that can be achieved by
administration of N-acetyl mannosamine and/or a derivative thereof
include improved kidney function, reduction in protein excretion in
the urine, reduction in blood concentrations in the urine,
increased sialylation of podocalyxin, increased sialylation of
PSA-NCAM (and/or other tissue specific target glycoproteins), fewer
cystic tubular dilatations in the kidney cortex and in the kidney
medulla, less fusion and flattening of the podocyte foot processes,
greater number of open slit diaphragms in the kidneys, improvement
in the "finger shaping" of the kidney foot processes, improved
overall integrity of the GBM, increased Gne/Mnk protein expression
and Gne-epimerase activities.
[0030] ManNAc is a ubiquitous but rare monosaccharide involved in a
range of metabolic processes. It is uncharged and crosses membranes
readily. ManNAc is a constituent of numerous glycolipids and
glycoproteins, and is the first committed precursor for the
biosynthesis of N-acetylneuraminic (Neu5Ac, or sialic acid), which
consists of N-acetyl-D-mannosamine in an ether linkage with
D-pyruvic acid. ManNAc is formed from UDP-N-acetylglucosamine
(UDP-GlcNAc) by the action of UDP-GlcNAc 2-epimerase. ManNAc is
then phosphorylated by a specific kinase to ManNAc-6-P (FIG. 1).
ManNAc is situated in the sialic acid biosynthesis pathway after
the regulated, rate-limiting GNE step (FIG. 1), so its metabolism
is not subject to feedback inhibition. Residual MNK activity in
HIBM patients, or ancillary kinases such as GlcNAc kinase
(Hinderlich et al. Eur. J. Biochem. 252: 133-139 (1998)), might
convert ManNAc into ManNAc-6-phosphate for subsequent synthesis of
sialic acid. In fact, hyposialylated, Gne-deficient mouse embryonic
stem cells became resialylated after their growth medium was
supplemented with ManNAc (Schwarzkopf et al. Proc. Natl. Acad. Sci.
U.S.A. 99: 5267-70 (2002)). Furthermore, incubation of cultured
cells with "unnatural" ManNAc derivatives, i.e.,
N-levulinoylmannosamine (ManLev) or N-azidoacetyl-mannosamine
(ManNAz), resulted in incorporation of the downstream sialic acid
analogs (SiaLev or SiaNAz) into cell surface glycoconjugates
(Charter et al. Glycobiology 10: 1049-56 (2000)).
Hereditary Inclusion Body Myopathy (HIBM)
[0031] Studies of an Iranian-Jewish genetic isolate (Argov, et al.,
Neurology 60, 1519-1523 (2003)) indicate that HIBM is mapped to
chromosome 9p12-13. The causative gene for HIBM is GNE, coding for
the bifunctional enzyme
UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase.
Eisenberg, et al. (2001) Nat Genet 29, 83-87 (2001); Tanner, M. E.,
Bioorg Chem 33, 216-228 (2005); Stasche, et al. J Biol Chem 272,
24319-24324 (1997); Hinderlich, et al. J Biol Chem 272, 24313-24318
(1997); Jacobs, et al. Biochemistry 40, 12864-12874 (2001). The
function and feedback regulation of GNE/MNK is depicted in FIG. 1.
Distal Myopathy with Rimmed Vacuoles (DMRV) is a Japanese variant,
allelic to HIBM. Nishino et al. Neurology 59, 1689-1693 (2002);
Kayashima et al. J Hum Genet 47, 77-79 (2002); Hinderlich, et al.
Neurology 61, 145 (2003). Nearly twenty GNE mutations have been
reported in HIBM patients from different ethnic backgrounds, with
founder effects among the Iranian Jews and Japanese. Broccolini ,
et al. Hum Mutat 23, 632 (2004); Eisenberg, et al. Hum Mutat 21, 99
(2003); Tomimitsu, et al. Neurology 59, 451-454 (2002); Darvish, et
al. Mol Genet Metab 77, 252-256 (2002). The mutations causing HIBM
occur in the regions encoding either the epimerase domain or the
kinase domain. Most are missense mutations and result in decreased
enzyme GNE activity and underproduction of sialic acid. Sparks, et
al. Glycobiology 15, 1102-1110 (2005); Penner, et al. Biochemistry
45, 2968-2977 (2006).
[0032] Sialic acids are negatively charged terminal sugar moieties
added during the post-translational modification on oligosaccharide
chains of proteins and lipids to create glycoproteins and
glycolipids. Varki, Faseb J 11, 248-255 (1997); Varki et al. Anal
Biochem 137, 236-247 (1984). They act as molecular determinants of
specific biological processes such as cellular adhesion, cell-cell
interactions and signal transduction. Schauer, Glycoconj J 17,
485-499 (2000); Kelm et al. Int Rev Cytol 175, 137-240 (1997).
[0033] The pathophysiology of HIBM remains largely unknown, but the
dysfunction in GNE suggests that impaired sialylation of
glycoproteins is involved. Such a defect could influence cell-cell
interactions, intracellular trafficking, organelle biogenesis,
apoptosis and secretion. In fact, UDP-GlcNAc 2-epimerase regulates
sialylation of cell surface molecules (Keppler et al. Science 284:
1372-76 (1999)), and sialylation appears to be critical for mouse
development (Schwarzkopf et al. Proc Natl Acad Sci USA 99,
5267-5270 (2002)).
[0034] One hypothesis for the pathophysiology of HIBM involves
undersialylation of .alpha.-DG, an essential component of the
dystrophin-glycoprotein complex. Michele et al. Nature 418, 417-422
(2002); Michele et al. J Biol Chem 278, 15457-15460 (2003).
.alpha.-DG is heavily glycosylated with O-mannosyl glycans
(mannose-N-acetylglucosamine-galactose-sialic acid) linked to a
serine or threonine; these glycans are critical for .alpha.-DG's
interactions with laminin and other extracellular ligands. Aberrant
glycosylation of .alpha.-DG is the underlying biochemical defect in
several congenital muscular dystrophies, generally termed
"dystroglycanopathies," including Fukuyama's congenital muscular
dystrophy, Muscle-Eye-Brain disease, Walker-Warburg syndrome and
the congenital muscular dystrophies type C1C and C1D. Martin et
al., Glycobiology 13, 67R-75R (2003); Martin-Rendon, et al. Trends
Pharmacol Sci 24, 178-183 (2003). The inventors and others have
shown variable hyposialylation of .alpha.-DG and other
glycoproteins, such as Neural Crest Adhesion Molecule (NCAM), in
HIBM. Huizing et al. Mol Genet Metab 81, 196-202 (2004); Savelkoul
et al. Mol Genet Metab 88, 389-390 (2006); Sparks et al. BMC Neurol
7, 3 (2007); Broccolini et al. Neuromuscul Disord 15, 177-184
(2005); Ricci et al. Neurology 66, 755-758 (2006); Salama et al.
Biochem Biophys Res Commun 328, 221-226 (2005); Tajima et al. Am J
Pathol 166, 1121-1130 (2005).
[0035] However, prior to the present invention, the basic
pathogenic mechanisms of HIBM, an HIBM animal model, and an
effective therapy for HIBM were lacking. These issues are addressed
by the present invention through creation of a Gne gene-targeted
knockin mouse mimicking the M712T mutation of Iranian-Jewish HIBM
patients and through studies using this knockin mouse model that
have defined effective therapeutic methods.
[0036] A sequence for the mouse Gne protein is shown below (SEQ ID
NO:1).
TABLE-US-00001 1 MEKNGNNRKL RVCVATCNRA DYSKLAPIMF GIKTEPAFFE 41
LDVVVLGSHL IDDYGNTYRM IEQDDFDINT RLHTIVRGED 81 EAAMVESVGL
ALVKLPDVLN RLKPDIMIVH GDRFDALALA 121 TSAALMNIRI LHIEGGEVSG
TIDDSIRHAI TKLAHYHVCC 161 TRSAEQHLIS MCEDHDRILL AGCPSYDKLL
SAKNKDYMSI 201 IRMWLGDDVK CKDYIVALQH PVTTDIKHSI KMFELTLDAL 241
ISFNKRTLVL FPNIDAGSKE MVRVMRKKGI EHHPNFRAVK 281 HVPFDQFIQL
VAHAGCMIGN SSCGVREVGA FGTPVINLGT 321 RQIGRETGEN VLHVRDADTQ
DKILQALHLQ FGKQYPCSKI 361 YGDGNAVPRI LKFLKSIDLQ EPLQKKFCFP
PVKENISQDI 401 DHILETLSAL AVDLGGTNLR VAIVSMKGEI VKKYTQFNPK 441
TYEERISLIL QMCVEAAAEA VKLNCRILGV GISTGGRVNP 481 QEGVVLHSTK
LIQEWNSVDL RTPLSDTLHL PVWVDNDGNC 521 AAMAERKFGQ GKGQENFVTL
ITGTGIGGGI IHQHELIHGS 561 SFCAAELGHL VVSLDGPDCS CGSHGCIEAY
ASGMALQREA 601 KKLHDEDLLL VEGMSVPKDE AVGALHLIQA AKLGNVKAQS 641
ILRTAGTALG LGVVNILHTM NPSLVILSGV LASHYIHIVK 681 DVIRQQALSS
VQDVDVVVSD LVDPALLGAA SMVLDYTTRR 721 IH
[0037] When this Gne protein has the M712T mutation, the sequence
for Gne mutant protein arising from the Gne.sup.M712T mutation is
as follows (SEQ ID NO:2), where the methionine at position 712 has
been changed to a threonine (bold and underlined amino acid shown
below).
TABLE-US-00002 1 MEKNGNNRKL RVCVATCNRA DYSKLAPIMF GIKTEPAFFE 41
LDVVVLGSHL IDDYGNTYRM IEQDDFDINT RLHTIVRGED 81 EAAMVESVGL
ALVKLPDVLN RLKPDIMIVH GDRFDALALA 121 TSAALMNIRI LHIEGGEVSG
TIDDSIRHAI TKLAHYHVCC 161 TRSAEQHLIS MCEDHDRILL AGCPSYDKLL
SAKNKDYMSI 201 IRMWLGDDVK CKDYIVALQH PVTTDIKHSI KMFELTLDAL 241
ISFNKRTLVL FPNIDAGSKE MVRVMRKKGI EHHPNFRAVK 281 HVPFDQFIQL
VAHAGCMIGN SSCGVREVGA FGTPVINLGT 321 RQIGRETGEN VLHVRDADTQ
DKILQALHLQ FGKQYPCSKI 361 YGDGNAVPRI LKFLKSIDLQ EPLQKKFCFP
PVKENISQDI 401 DHILETLSAL AVDLGGTNLR VAIVSMKGEI VKKYTQFNPK 441
TYEERISLIL QMCVEAAAEA VKLNCRILGV GISTGGRVNP 481 QEGVVLHSTK
LIQEWNSVDL RTPLSDTLHL PVWVDNDGNC 521 AAMAERKFGQ GKGQENFVTL
ITGTGIGGGI IHQHELIHGS 561 SFCAAELGHL VVSLDGPDCS CGSHGCIEAY
ASGMALQREA 601 KKLHDEDLLL VEGMSVPKDE AVGALHLIQA AKLGNVKAQS 641
ILRTAGTALG LGVVNILHTM NPSLVILSGV LASHYIHIVK 681 DVIRQQALSS
VQDVDVVVSD LVDPALLGAA STVLDYTTRR 721 IH
[0038] Although this M712T mutation gives rise to a recessive
phenotype, it has dramatic effects upon the survival and physiology
of mammals. For example, HIBM exhibits non life-threatening
symptoms in humans that emerge in adulthood and lead to slowly
progressive muscle weakness. Most patients develop symptoms while
in their early 20s and become wheelchair-bound by the time they
reach 40, as their arm, hand, leg and core muscles progressively
weaken. The symptoms in mice are even more dramatic. For example,
upon mating nine pairs of Gne.sup.M712T/+ mice, 101 progeny were
obtained. Of those 101 progeny 26 homozygous mutated
(Gne.sup.M712T/M712T) mice were produced. However, only one male
with the Gne.sup.M712T/M712T genotype survived past age P3 (FIG.
2D). The remaining 25 Gne.sup.M712T/M712T homozygous mutated
offspring died at age P1-P3. This lone surviving mouse showed no
muscle pathology at age P2. The lack of early myopathic features
recapitulates the human HIBM phenotype. In both mice and humans,
the muscle pathology occurs late or is attenuated likely by a
modicum of sialic acid is provided through the actions of residual
Gne/Mnk enzymatic activities (Sparks et al. Glycobiology 15:
1102-10 (2005); Noguchi et al. J. Biol. Chem. 279: 11402-407
(2004)) (FIG. 5F and FIGS. 6, A and B).
Kidney Conditions
[0039] Instead of early-onset muscle problems, homozygous
Gne.sup.M712T/M712T mice exhibit early signs of severe glomerular
hematuria and podocytopathy, including effacement of the podocyte
foot processes and segmental splitting of the glomerular basement
membrane (GBM), likely due to hyposialylation of specific membrane
glycoproteins. Unexpectedly, the Gne.sup.M712T/M712T knockin mice
provide a novel animal model of podocytopathy and/or segmental
splitting of the GBM, demonstrating the significance of sialic acid
synthesis in kidney development and function. Structural elements
in the kidney that are important for filtering waste from the blood
are severely impaired by the sialic acid deficiency. This outcome
demonstrates the significance of the ability of the body to
synthesize sialic acid for kidney development and function.
[0040] As shown in the Examples and Figures of this application,
administration of ManNAc to pregnant mice had a remarkably salutary
effect on the survival and renal development of homozygous pups. In
particular, ManNAc administration was associated with increased
enzymatic activity of Gne, increased sialylation of kidney
podocalyxin, and improved morphology of the podocyte foot processes
and GBM integrity.
[0041] Therefore, according to the invention, ManNAc is effective
not only as a treatment for HIBM but also for treatment of kidney
disorders. Thus, ManNAc may be used to treat podocytopathies,
minimal change nephrosis, focal and segmental glomerulosclerosis,
membranous glomerulonephritis, and other forms of unexplained
idiopathic nephrotic syndrome, as well as glomerular basement
membrane diseases such as Alport disease and thin membrane disease.
Such kidney disorders and conditions are sometimes characterized by
segmental splitting of the glomerular basement membrane and/or
podocytopathy due to disturbed polyanions on podocyte membranes, or
to changes in the amount or charge (sialylation) of glomerular
basement membrane components.
Formulations and Administration
[0042] N-acetyl mannosamine and/or derivatives thereof are
administered so as to achieve a reduction in at least one symptom
associated with an indication or disease. For example,
administration of N-acetyl mannosamine and/or derivatives thereof
can lead to a reduction in proteinuria (e.g., lower amounts of
protein in the urine), a reduction in hematuria (e.g., lower
amounts of red blood cells in the urine) and improvement of muscle
function (e.g., in patients with muscular atrophy).
[0043] To achieve the desired effect(s), N-acetyl mannosamine
and/or derivatives thereof may be administered as single or divided
dosages, for example, of at least about 0.01 mg/kg to about 500 to
750 mg/kg, of at least about 0.01 mg/kg to about 300 to 500 mg/kg,
at least about 0.1 mg/kg to about 200 to 400 mg/kg or at least
about 1 mg/kg to about 25 to 200 mg/kg of body weight, although
other dosages may provide beneficial results. The amount
administered will vary depending on various factors including, but
not limited to the disease, the weight, the physical condition, the
health, the age of the mammal, whether prevention or treatment is
to be achieved. Such factors can be readily determined by the
clinician employing animal models or other test systems that are
available in the art.
[0044] Administration of the therapeutic agents in accordance with
the present invention may be in a single dose, in multiple doses,
in a continuous or intermittent manner, depending, for example,
upon the recipient's physiological condition, whether the purpose
of the administration is therapeutic or prophylactic, and other
factors known to skilled practitioners. The administration of
N-acetyl mannosamine and/or derivatives thereof may be essentially
continuous over a pre-selected period of time or may be in a series
of spaced doses. Both local and systemic administration is
contemplated.
[0045] To prepare the composition, N-acetyl mannosamine and/or one
or more derivatives thereof are synthesized or otherwise obtained,
and purified as necessary or desired. N-acetyl mannosamine (and/or
derivatives thereof) can then be added to a composition (or food
product), adjusted to the appropriate concentration, and optionally
combined with other agents. The absolute weight of N-acetyl
mannosamine and/or its derivatives that is included in a unit dose
can vary widely. For example, about 0.01 to about 2 g, or about 0.1
to about 1 g of N-acetyl mannosamine and/or derivatives thereof are
often used in compositions. Alternatively, the unit dosage can vary
from about 0.01 g to about 50 g, from about 0.01 g to about 35 g,
from about 0.1 g to about 25 g, from about 0.5 g to about 12 g,
from about 0.5 g to about 8 g, from about 0.5 g to about 4 g, or
from about 0.5 g to about 2 g.
[0046] Daily doses of N-acetyl mannosamine and/or derivatives
thereof can vary as well. Such daily doses can range, for example,
from about 0.1 g/day to about 50 g/day, from about 0.2 g/day to
about 25 g/day, from about 0.3 g/day to about 12 g/day, from about
0.4 g/day to about 10 g/day, from about 0.5 g/day to about 8 g/day,
and from about 0.7 g/day to about 6 g/day.
[0047] Thus, one or more suitable unit dosage forms comprising
N-acetyl mannosamine and/or derivatives thereof can be administered
by a variety of routes including oral, parenteral (including
subcutaneous, intravenous, intramuscular and intraperitoneal),
rectal, dermal, transdermal, intrathoracic, intrapulmonary and
intranasal (respiratory) routes. The therapeutic agents may also be
formulated for sustained release (for example, using
microencapsulation, see WO 94/07529, and U.S. Pat. No. 4,962,091).
The formulations may, where appropriate, be conveniently presented
in discrete unit dosage forms and may be prepared by any of the
methods well known to the pharmaceutical arts. Such methods may
include the step of mixing N-acetyl mannosamine and/or derivatives
thereof with liquid carriers, solid matrices, semi-solid carriers,
finely divided solid carriers or combinations thereof, and then, if
necessary, introducing or shaping the product into the desired
delivery system.
[0048] When N-acetyl mannosamine and/or its derivatives is prepared
for oral administration, it is generally combined with a
pharmaceutically acceptable carrier, diluent or excipient to form a
pharmaceutical formulation, or unit dosage form. For oral
administration, N-acetyl mannosamine (and/or derivatives thereof)
may be present as a powder, a granular formulation, a solution, a
suspension, an emulsion or in a natural or synthetic polymer or
resin for ingestion of N-acetyl mannosamine (and/or one or more
derivatives thereof) from a chewing gum. The active ingredients may
also be presented as a bolus, electuary or paste. Orally
administered N-acetyl mannosamine and/or derivatives thereof can
also be formulated for sustained release. For example, N-acetyl
mannosamine and/or derivatives thereof can be coated,
micro-encapsulated, or otherwise placed within a sustained delivery
device, for example, in order to avoid salivary bacteria
degradation. The total N-acetyl mannosamine and its derivatives in
such formulations comprises from 0.1 to 99.9% by weight of the
formulation.
[0049] By "pharmaceutically acceptable" it is meant a carrier,
diluent, excipient, and/or salt that is compatible with the other
ingredients of the formulation, and not deleterious to the
recipient thereof.
[0050] Pharmaceutical formulations containing N-acetyl mannosamine
and/or derivatives thereof can be prepared by procedures known in
the art using well-known and readily available ingredients. For
example, N-acetyl mannosamine and/or its derivatives can be
formulated with common excipients, diluents, or carriers, and
formed into tablets, capsules, solutions, suspensions, powders,
aerosols and the like. Examples of excipients, diluents, and
carriers that are suitable for such formulations include buffers,
as well as fillers and extenders such as starch, cellulose, sugars,
mannitol, and silicic derivatives. Binding agents can also be
included such as carboxymethyl cellulose, hydroxymethylcellulose,
hydroxypropyl methylcellulose and other cellulose derivatives,
alginates, gelatin, and polyvinyl-pyrrolidone. Moisturizing agents
can be included such as glycerol, disintegrating agents such as
calcium carbonate and sodium bicarbonate. Agents for retarding
dissolution can also be included such as paraffin. Resorption
accelerators such as quaternary ammonium compounds can also be
included. Surface active agents such as cetyl alcohol and glycerol
monostearate can be included. Adsorptive carriers such as kaolin
and bentonite can be added. Lubricants such as talc, calcium and
magnesium stearate, and solid polyethyl glycols can also be
included. Preservatives may also be added. The compositions of the
invention can also contain thickening agents such as cellulose
and/or cellulose derivatives. They may also contain gums such as
xanthan, guar or carbo gum or gum arabic, or alternatively
polyethylene glycols, bentones and montmorillonites, and the
like.
[0051] For example, tablets or caplets containing N-acetyl
mannosamine (and/or its derivatives) can include buffering agents
such as calcium carbonate, magnesium oxide and magnesium carbonate.
Caplets and tablets can also include inactive ingredients such as
cellulose, pre-gelatinized starch, silicon dioxide, hydroxy propyl
methyl cellulose, magnesium stearate, microcrystalline cellulose,
starch, talc, titanium dioxide, benzoic acid, citric acid, corn
starch, mineral oil, polypropylene glycol, sodium phosphate, zinc
stearate, and the like. Hard or soft gelatin capsules containing
N-acetyl mannosamine (and/or its derivatives) can contain inactive
ingredients such as gelatin, microcrystalline cellulose, sodium
lauryl sulfate, starch, talc, and titanium dioxide, and the like,
as well as liquid vehicles such as polyethylene glycols (PEGs) and
vegetable oil. Moreover, enteric-coated caplets or tablets
containing N-acetyl mannosamine and/or its derivatives are designed
to resist disintegration in the stomach and dissolve in the more
neutral to alkaline environment of the duodenum.
[0052] N-acetyl mannosamine and/or its derivatives can also be
formulated as an elixir or solution for convenient oral
administration or as a solution appropriate for parenteral
administration, for instance by intramuscular, subcutaneous,
intraperitoneal or intravenous routes. The pharmaceutical
formulations of N-acetyl mannosamine and/or its derivatives can
also take the form of an aqueous or anhydrous solution or
dispersion, or alternatively the form of an emulsion or suspension
or salve.
[0053] Thus, N-acetyl mannosamine and/or its derivatives may be
formulated for parenteral administration (e.g., by injection, for
example, bolus injection or continuous infusion) and may be
presented in unit dose form in ampoules, pre-filled syringes, small
volume infusion containers or in multi-dose containers. As noted
above, preservatives can be added to help maintain the shelve life
of the dosage form. The N-acetyl mannosamine, its derivatives and
other ingredients may form suspensions, solutions, or emulsions in
oily or aqueous vehicles, and may contain formulatory agents such
as suspending, stabilizing and/or dispersing agents. Alternatively,
the N-acetyl mannosamine, its derivatives and other ingredients may
be in powder form, obtained by aseptic isolation of sterile solid
or by lyophilization from solution, for constitution with a
suitable vehicle, e.g., sterile, pyrogen-free water, before
use.
[0054] These formulations can contain pharmaceutically acceptable
carriers, vehicles and adjuvants that are well known in the art. It
is possible, for example, to prepare solutions using one or more
organic solvent(s) that is/are acceptable from the physiological
standpoint, chosen, in addition to water, from solvents such as
acetone, ethanol, isopropyl alcohol, glycol ethers such as the
products sold under the name "Dowanol," polyglycols and
polyethylene glycols, C.sub.1-C.sub.4 alkyl esters of short-chain
acids, ethyl or isopropyl lactate, fatty acid triglycerides such as
the products marketed under the name "Miglyol," isopropyl
myristate, animal, mineral and vegetable oils and
polysiloxanes.
[0055] It is possible to add other ingredients such as
antioxidants, surfactants, other preservatives, film-forming,
keratolytic or comedolytic agents, perfumes, flavorings and
colorings. Antioxidants such as t-butylhydroquinone, butylated
hydroxyanisole, butylated hydroxytoluene and .alpha.-tocopherol and
its derivatives can be added.
[0056] Additionally, N-acetyl mannosamine and/or derivatives
thereof are well suited to formulation in a sustained release
dosage form. Thus, such formulations can be so constituted that
they release the N-acetyl mannosamine and/or its derivative, for
example, in a particular part of the intestinal, urogenital or
respiratory tract, over a period of time. Coatings, envelopes, and
protective matrices may be made, for example, from polymeric
substances, such as polylactide-glycolates, liposomes,
microemulsions, microparticles, nanoparticles, or waxes. These
coatings, envelopes, and protective matrices are useful to coat
indwelling devices, e.g., stents, catheters, peritoneal dialysis
tubing, draining devices and the like.
[0057] For topical administration, N-acetyl mannosamine and/or its
derivative(s) may be formulated as is known in the art for direct
application to a target area. Forms chiefly conditioned for topical
application take the form, for example, of creams, milks, gels,
dispersion or microemulsions, lotions thickened to a greater or
lesser extent, impregnated pads, ointments or sticks, aerosol
formulations (e.g., sprays or foams), soaps, detergents, lotions or
cakes of soap. Other conventional forms for this purpose include
wound dressings, coated bandages or other polymer coverings,
ointments, creams, lotions, pastes, jellies, sprays, and aerosols.
Thus, N-acetyl mannosamine and/or its derivatives can be delivered
via patches or bandages for dermal administration. Alternatively,
N-acetyl mannosamine and/or its derivatives can be formulated to be
part of an adhesive polymer, such as polyacrylate or acrylate/vinyl
acetate copolymer. For long-term applications it might be desirable
to use microporous and/or breathable backing laminates, so
hydration or maceration of the skin can be minimized. The backing
layer can be any appropriate thickness that will provide the
desired protective and support functions. A suitable thickness will
generally be from about 10 to about 200 microns.
[0058] Ointments and creams may, for example, be formulated with an
aqueous or oily base with the addition of suitable thickening
and/or gelling agents. Lotions may be formulated with an aqueous or
oily base and will in general also contain one or more emulsifying
agents, stabilizing agents, dispersing agents, suspending agents,
thickening agents, or coloring agents. The therapeutic agents can
also be delivered via iontophoresis, e.g., as disclosed in U.S.
Pat. Nos. 4,140,122; 4,383,529; or 4,051,842. The percent by weight
of a therapeutic agent of the invention present in a topical
formulation will depend on various factors, but generally will be
from 0.01% to 95% of the total weight of the formulation, and
typically 0.1-85% by weight.
[0059] Drops, such as eye drops or nose drops, may be formulated
with N-acetyl mannosamine and/or derivatives thereof in an aqueous
or non-aqueous base also comprising one or more dispersing agents,
solubilizing agents or suspending agents. Liquid sprays are
conveniently delivered from pressurized packs. Drops can be
delivered via a simple eye dropper-capped bottle, or via a plastic
bottle adapted to deliver liquid contents dropwise, via a specially
shaped closure.
[0060] N-acetyl mannosamine and/or its derivatives may further be
formulated for topical administration in the mouth or throat. For
example, N-acetyl mannosamine and/or its derivatives may be
formulated as a lozenge further comprising a flavored base, usually
sucrose and acacia or tragacanth; pastilles comprising the
composition in an inert base such as gelatin and glycerin or
sucrose and acacia; and mouthwashes comprising the composition of
the present invention in a suitable liquid carrier.
[0061] The pharmaceutical formulations of the present invention may
include, as optional ingredients, pharmaceutically acceptable
carriers, diluents, solubilizing or emulsifying agents, and salts
of the type that are available in the art.
[0062] Furthermore, N-acetyl mannosamine and/or its derivatives may
also be used in combination with other therapeutic agents, for
example, pain relievers, anti-inflammatory agents, and the like,
whether for the conditions described or some other condition.
[0063] The present invention further pertains to a packaged
pharmaceutical composition such as a kit or other container for
increasing production of sialic acid in a mammal. The kit or
container holds a therapeutically effective amount of a
pharmaceutical composition for increasing intracellular production
of sialic acid and instructions for using the pharmaceutical
composition for increasing production of sialic acid in the mammal.
The pharmaceutical composition includes N-acetyl mannosamine and/or
its derivatives in a therapeutically effective amount such that
sialic acid production is increased.
Food Supplement
[0064] According to the invention, N-acetyl mannosamine and/or its
derivatives can be administered as a food supplement or
incorporated into food or drink item such as a nutritional bar,
snack bar, cookie, candy, cereal, pudding, ice cream, frozen
confectionary, chewing gum, drink mix, soda pop, liquid supplement,
sauce, salad dressing, gravy, jelly, jam, spread, margarine, peanut
butter, nut spread, frosting, and the like. In essence, can be used
in any food, composition or supplement in which sugar is employed.
Hence, N-acetyl mannosamine and/or derivatives thereof can be used
as a partial or full substitute for sugar.
[0065] Such food supplements, drinks and food items can include any
other food ingredient including, for example, flour, oil, cream,
butter, sugar, salt, spices and the like. In addition, the food
supplements, drinks and food items can include vitamins and
nutrients commonly found in other nutritional supplements.
[0066] Having now generally described the invention, the same will
be more readily understood through reference to the following
examples which are provided by way of illustration, and are not
intended to be limiting of the present invention.
EXAMPLE 1
ManNAc Administration is Useful for Treating HIBM and Renal
Disorders
[0067] This Example shows that ManNAc may be a useful treatment not
only for HIBM but also for renal disorders involving proteinuria
and hematuria due to podocytopathy and/or segmental splitting of
the glomerular basement membrane.
Methods
[0068] Gne.sup.M712T/M712T mice. Gne.sup.M712T/M712T knockin mice
were generated by targeting the M712T (ATG to ACG) mutation of exon
12 of the murine Gne gene (Gne, Uae1, GenBank NM_015828) (FIG. 2A).
The nucleotide sequence for this Gne, Uae1 allele (GenBank
NM_015828) without the mutation is shown below for easy reference
(SEQ ID NO:3).
TABLE-US-00003 1 GCTAAACCAG AGGCCAGACG GCAGCTCAGG AGTCCGACCA 41
CACCTCAGGA AACAGCTGTG CCACAGGATG GAAACACACG 81 CGCATCTCCA
CAGGGAGCAG AGCTACGCAG GACCTCATGA 121 ACTCTATTTT AAGAAACTCT
CAAGTAAAAA GAAGCAAGTC 161 ATGGAGAAGA ACGGGAACAA CCGAAAGCTC
CGGGTTTGCG 201 TTGCCACCTG CAACCGAGCT GACTACTCCA AACTGGCCCC 241
GATCATGTTC GGCATCAAGA CAGAGCCCGC GTTCTTTGAG 281 TTGGACGTGG
TGGTGCTCGG CTCCCACCTG ATTGACGACT 321 ATGGAAACAC ATACCGCATG
ATTGAGCAAG ATGACTTTGA 361 CATTAACACC AGGCTCCACA CGATTGTTAG
AGGGGAAGAT 401 GAAGCGGCCA TGGTAGAGTC GGTAGGCCTA GCGCTCGTGA 441
AGCTACCGGA CGTCCTCAAT CGCCTGAAGC CCGACATCAT 481 GATTGTTCAC
GGAGACCGAT TTGACGCCCT TGCTCTGGCT 521 ACGTCTGCTG CCTTGATGAA
CATCCGCATC CTTCACATTG 561 AAGGAGGCGA GGTCAGCGGG ACCATTGATG
ACTCTATCAG 601 ACACGCCATA ACAAAACTGG CTCACTACCA TGTGTGCTGC 641
ACTAGAAGTG CAGAGCAGCA CCTGATCTCT ATGTGCGAGG 661 ACCACGACCG
CATCCTGTTG GCAGGCTGCC CTTCCTATGA 721 CAAACTGCTC TCCGCCAAGA
ACAAAGACTA TATGAGCATC 761 ATTCGGATGT GGCTAGGCGA TGATGTAAAA
TGTAAGGATT 801 ACATCGTTGC CCTGCAGCAT CCCGTGACCA CTGACATTAA 841
GCATTCCATA AAGATGTTTG AGCTAACACT GGATGCCCTG 881 ATCTCGTTTA
ACAAGAGGAC CCTAGTTCTG TTTCCAAATA 921 TCGATGCAGG CAGCAAGGAG
ATGGTTCGAG TGATGCGGAA 961 GAAGGGCATC GAGCATCACC CCAATTTCCG
TGCAGTCAAG 1001 CACGTCCCGT TTGACCAGTT CATACAGCTG GTCGCCCACG 1041
CTGGCTGCAT GATTGGGAAT AGCAGCTGCG GCGTGCGAGA 1081 GGTTGGCGCT
TTCGGAACAC CCGTGATCAA CCTGGGCACA 1121 AGGCAGATAG GAAGAGAAAC
CGGGGAGAAT GTTCTTCATG 1161 TCAGGGATGC TGACACCCAA GATAAAATAT
TGCAAGCACT 1201 ACACCTCCAG TTCGGCAAAC AGTACCCTTG CTCAAAGATA 1241
TATGGGGATG GGAATGCTGT TCCAAGGATT TTAAAGTTTC 1281 TCAAATCCAT
TGACCTTCAA GAGCCACTAC AGAAGAAATT 1321 CTGCTTCCCC CCTGTAAAGG
AGAACATCTC TCAAGACATT 1361 GACCACATCC TGGAAACTCT GAGTGCCTTG
GCTGTTGATC 1401 TTGGCGGGAC AAACCTGAGG GTGGCAATAG TTAGCATGAA 1441
GGGTGAAATC GTTAAGAAGT ACACTCAGTT CAACCCTAAA 1481 ACCTATGAAG
AAAGGATTAG TTTAATCCTG CAGATGTGTG 1521 TGGAAGCTGC CGCGGAAGCT
GTGAAACTCA ATTGCAGAAT 1561 TCTGGGAGTA GGCATCTCCA CAGGTGGCCG
CGTGAATCCC 1601 CAGGAAGGAG TTGTGCTGCA TTCAACCAAG CTGATCCAGG 1641
AATGGAACTC CGTGGACCTC AGGACACCCC TCTCCGACAC 1681 CCTGCATCTC
CCCGTGTGGG TGGACAATGA CGGCAACTGT 1721 GCCGCCATGG CAGAGAGGAA
GTTCGGCCAA GGAAAAGGAC 1761 AGGAGAACTT CGTGACGCTC ATCACGGGGA
CAGGGATCGG 1801 TGGGGGGATC ATCCACCAGC ACGAACTGAT CCACGGCAGC 1841
TCCTTCTGCG CGGCGGAGCT CGGCCATCTC GTGGTGTCCC 1881 TGGACGGTCC
TGACTGCTCC TGTGGAAGCC ATGGGTGCAT 1921 CGAAGCGTAC GCCTCTGGAA
TGGCCTTGCA GAGGGAAGCA 1961 AAGAAACTCC ATGATGAGGA CCTGCTCTTG
GTGGAAGGGA 2001 TGTCAGTACC AAAAGACGAA GCTGTGGGTG CCCTCCATCT 2041
CATCCAGGCT GCCAAGCTGG GCAACGTGAA GGCCCAGAGC 2081 ATCTTACGAA
CAGCTGGAAC TGCTTTGGGA CTTGGGGTTG 2121 TGAACATCCT CCACACTATG
AATCCTTCCC TGGTGATCCT 2161 GTCTGGAGTC CTGGCCAGTC ACTACATCCA
CATCGTGAAG 2201 GACGTCATCC GCCAGCAAGC CTTGTCCTCC GTGCAGGATG 2241
TGGACGTGGT GGTCTCAGAC TTGGTGGACC CGGCCCTGCT 2281 TGGCGCAGCC
AGCATGGTTC TGGACTACAC AACGCGCAGG 2321 ATCCACTAGG TCTCCCGGGA
ACGGACACGG ACAGAGACTC 2361 GGGAGCTGCT TAGAGTGGAA CCATGCTCTT
CTAGATCAGT 2401 GTTTCTGCGA AGGCAAATTT GGGGGGAGGG CTGCTGAGAC 2441
AGCTCAGTGG TTAAGAGCCT GCCCTGCTCC TGCCAGTCCC 2481 CAGCACCCAT
GTCAGGCAGC TCAGCTGCCT GGAAGCCAAG 2521 CTCCAGGGGA CCCAATGCCT
CTCTGCCGGG GGCAGCTGCA 2561 CTCAGATGTA CATACCCCTC TCCACACACA
TACAAATAAA 2601 GCTTATTTTT CAAAAGGCAA AAAAAAAAAA AAAAAAAAAA 2641
AAAAAAAAAA AAAA
The mutant mice were maintained in the C57BL/6J background. Animals
were housed in an accredited specific pathogen-free facility in
accordance with accepted guidelines. Cages were ventilated in a
temperature- and light-controlled environment (22.degree. C.,
30%-70% humidity, 12-hour light/12-hour dark cycle). The mice were
fed irradiated chow (Prolab 5P75 Isopro 3000; PMI Nutrition
International) and sterile water ad libitum. All euthanasia was
performed by CO.sub.2 inhalation followed by cervical
dislocation.
[0069] For Mendelian distribution studies, 4 pregnant mice at
E17-E19 were euthanized, and embryos were retrieved by cesarean
section and euthanized by decapitation. All mouse procedures were
performed in accordance with protocol G04-3 and were approved by
the Institutional Animal Care and Use Committee of the National
Human Genome Research Institute.
[0070] Molecular analysis. Mouse genotyping was performed on tail
genomic DNA or cDNA isolated from kidney or skeletal muscle using
standard protocols. Total RNA was isolated from murine tissues
using the TRIzol reagent (Invitrogen), and cDNA was prepared using
the SuperScript III system (Invitrogen). PCR amplifications were
performed across the M712T mutation with genomic DNA as template,
using the primer set 5'- agcacttcctgagtttgatg-3' (SEQ ID NO:4) and
5'-atttgccttcgcaga-cacttga-3' (SEQ ID NO:5) (FIG. 2B) or with cDNA
as template (FIG. 2C), using the primer set
5'-GCCCAGAGCATCTTACGAAC-3' (SEQ ID NO:6) and
5'-GGGTCCCCTGGAGCTTGG-3' (SEQ ID NO:7) and PuReTaq Ready-To-Go PCR
beads (GE Healthcare), using standard PCR conditions. PCR fragments
were digested with Nla III at 37.degree. C. to verify the mutation
status (FIGS. 2B and C). Quantitative realtime PCR was performed on
RNA isolated from kidney and skeletal muscle, utilizing
Assays-On-Demand (Applied Biosystems) for Gne (mm00607939), Pecam-1
(mm00476702), Col4A3 (mm01269206), and .beta.-actin (mm00450174) on
an ABI PRISM 7900 HT Sequence Detection System (Applied
Biosystems).
[0071] Clinical chemistry screen. Retroorbital blood samples
(100-150 ml) from weaned mice (weighing at least 15 grams) matched
for sex (male) and age were obtained bimonthly after pretreatment
with a topical anesthetic (0.5% tetracaine HCl; Bausch & Lomb
Pharmaceuticals). Samples were allowed to clot (30 minutes at room
temperature) in MicroPrep centrifuge tubes (IRIS International
Inc.), after which the serum was separated by centrifugation at
1500 g for 10 minutes and stored at -80.degree. C. until analysis.
Clinical chemistry screens were performed at the Department of
Laboratory Medicine at the NIH and included monitoring of
creatinine, blood urea nitrogen, albumin, total protein, uric acid,
alkaline phosphatase, alanine aminotransferase, aspartate
aminotransferase, amylase, creatine kinase, and lactate
dehydrogenase. In addition, reagent strips for protein urinalysis
were used to assess proteinuria (Chemstrip 2GP; Roche
Diagnostics).
[0072] Antibodies. A rabbit polyclonal antibody was custom prepared
against a Gne/Mnk peptide comprising amino acids 588-607
(EAYASGMALQREAKKLHDED, SEQ ID NO:8), coupled to keyhole limpet
hemocyanine, and affinity purified against the corresponding
antigenic peptide (Covance). The following additional primary
antibodies were commercially obtained: dystrophin (catalog no.
ab15277; Abcam); .alpha.-dystroglycan (clone IIH6C4; Upstate
Biotechnology); laminin-1 (catalog no. L9393; Sigma-Aldrich);
podocalyxin (catalog no. PODX11-A; Alpha Diagnostic International);
podocin (catalog no. P0372; Sigma-Aldrich); laminin .beta.1
(catalog no. MAB1928; Millipore); desmin (catalog no. 1466-1;
Epitomics); a-SMA (SPM332; GeneTex Inc.); PSA-NCAM (catalog no.
MAB5324; Millipore); and .beta.-actin (catalog no. AAN01;
Cytoskeleton).
[0073] Mouse histology. Mouse tissues were collected, formalin
fixed (10%) and paraffin embedded. Tissue sections (5 mm) were
stained with H&E following standard procedures (American
Histolabs) or subjected to immunohistochemistry with a variety of
primary antibodies. Formalin-fixed tissues were deparaffinized in
HistoClear II (National Diagnostics) and dehydrated in a series of
ethanol solutions. Antigen retrieval was performed for sections
that were to be stained with antibodies against Gne/Mnk (by boiling
5 minutes in citric acid-based solution; Vector Laboratories) and
against dystrophin (by boiling in 1 mM EDTA according the
manufacturer's protocol; AbCam). The sections were blocked (2% BSA,
10% donkey serum, and 0.1% Triton X-100 in PBS) and incubated with
primary antibodies (Gne/Mnk 1:50; laminin 1:25; dystrophin 1:50)
overnight at 4.degree. C., followed by incubation with the
secondary antibody, Alexa Fluor 488-conjugated donkey anti-rabbit
(1:500 in blocking solution) (Invitrogen). The sections were
mounted in VECTASHIELD Mounting Medium (Vector Laboratories) and
viewed and digitally imaged with a Zeiss Axiovert 200M microscope
(Zeiss).
[0074] Western blotting. Mouse tissues (age P2) were extracted,
homogenized in CelLytic buffer consisting of a mild detergent,
bicine buffer, and 150 mM NaCl (Sigma-Aldrich) supplemented with
protease inhibitors (Complete Mini; Roche Applied Science). The
lysates were sonicated and cleared by centrifugation (1000 g for 10
minutes), and the resulting supernatants were assayed for protein
(BCA Protein Assay; Pierce Biotechnology). For the neuraminidase
enzymatic treatments (FIG. 6E), protein homogenates (25 mg) were
incubated for 30 min at 37.degree. C. with 1 mU/mg of neuraminidase
(catalog no. N6514; Sigma-Aldrich). Equal amounts of protein (25-50
mg) were electrophoresed on 4%-12% Tris-Glycine gels (Novex;
Invitrogen), and electroblotted onto 0.45 mm Hybond ECL
nitrocellulose membranes (GE Healthcare). The membranes were
blocked (10% fat-free milk) and incubated with primary antibodies
followed by HRP-conjugated secondary antibodies (GE Healthcare).
Results were visualized with ECL (ECL Western Blotting Detection
Reagents; GE Healthcare) and exposure to CL-XPosure Film (Pierce
Biotechnology). Densitometry was performed on the digital images
obtained with a Kodak Image Station and software (PerkinElmer). The
protein levels were normalized to those of .beta.-actin to correct
for differences in protein loading and/or transfer.
[0075] Electron microscopy. Kidney samples were fixed overnight at
4.degree. C. in 2% glutaraldehyde in 0.1 M cacodylate buffer (pH
7.4) and washed with cacodylate buffer. After postfixation with 1%
OsO4 for 2 hours and a second wash with 0.1 M cacodylate buffer,
the tissues were serially dehydrated in ethanol and embedded in
Eponate 12 resin (Ted Pella). Thin sections (.about.80 nm) were
obtained using a Leica Ultracut UCT Ultramicrotome (Leica
Microsystems), placed onto 400 mesh copper grids, and stained with
saturated uranyl acetate in 50% methanol followed by lead citrate.
The grids were viewed with a Philips 410 electron microscope (FEI
Company) at 80 kV, and images were recorded on Kodak SO-163 film
(Kodak).
[0076] ManNAc administration. Breeding pairs of 6-week-old
Gne.sup.M712T/+ mice were divided into 3 groups. Group I consisted
of 9 Gne.sup.M712T/+ breeding pairs, who were administered
untreated sterilized tap water. Group II consisted of 1 breeding
pair of Gne.sup.+/+ mice (wild-type control) and 6 Gne.sup.M712T/+
breeding pairs, who were administered water containing 1 mg/ml
(.about.0.2 g/kg/day) ManNAc (Sigma-Aldrich). That dose was
selected based on previous evidence of the safety of ManNAc
(administered at a single dose of 0.142 g/kg/day) in a study
performed in humans (21). Group III consisted of 1 Gne.sup.+/+
breeding pair and 7 Gne.sup.M712T/+ breeding pairs, who were
administered water supplemented with 5 mg/ml (.about.1.0 g/kg/day)
ManNAc. Water was changed twice weekly. Nursing females continued
to be supplied with ManNAc. All mice were weaned from ManNAc at 21
days. Selected whole litters were euthanized at age P2, P6, and P19
for histological, genetic, biochemical, or ultrastructural
analysis.
[0077] Gne enzymatic assays. Mouse kidney and skeletal muscle
(quadriceps) tissues were homogenized and subjected to the
Gne-epimerase enzymatic assay as previously described (11, 58).
This assay was based on incubation with radiolabeled substrate
(Uridine diphosphate N-acetyl glucosamine [1-.sup.3H]; American
Radiolabeled Chemicals Inc.) and detection of radiolabeled product
([.sup.3H]ManNAc) upon separation of oligosaccharides by high-pH
anion-exchange chromatography with pulsed amperometric detection
(Dionex).
[0078] Statistics. Differences between data groups were evaluated
for significance using the 2-tailed Student's t test of unpaired
data. For Mendelian distribution analysis, a goodness-of-fit
(.chi.2) test was performed, while for comparisons of survival
between treated and untreated mice of all genotypes (Gne.sup.+/+,
Gne.sup.M712T/+, and Gne.sup.M712T/M712T), a 2-tailed Fisher's
exact test using a 2.times.3 table was employed. All data are
presented as the mean.+-.SD. A P value less than 0.05 was
considered statistically significant.
Results
[0079] Generation of Gne.sup.M712T/M712T knockinn mice. A murine
targeting vector for homologous recombination in C57BL/6J embryonic
stem cells was constructed to include the M712T Gne mutation (FIG.
2A). The neomycin phosphotransferase and thymidine kinase genes
were introduced into the vector as positive and negative selection
markers, respectively (FIG. 2A). Additional LoxP (flanking exon 12
and neo) and flippase recombinase target sites (flanking neo) were
inserted for transgenic models for this condition (Nagy, A. 2000.
Cre recombinase: the universal reagent for genome tailoring.
Genesis. 26:99-109). The entire vector was sequence verified.
Genotyping of the mice was performed by PCR amplification and
digestion with the restriction endonuclease NlaIII (FIG. 2B).
Tissues of homozygous mutant Gne.sup.M712T/M712T and wild-type
Gne.sup.+/+ mice showed comparable Gne RNA transcript levels by
real-time quantitative PCR. Furthermore, NlaIII digestion of
amplified cDNA demonstrated homozygous insertion of the M712T
mutation in RNA of Gne.sup.M712T/M712T mice (FIG. 2C).
[0080] Early postnatal lethality. Initial matings of heterozygous
mice (Gne.sup.M712T/+) yielded 101 offspring from which only 1
Gne.sup.M712T/M712T animal survived beyond P21. The remaining
Gne.sup.M712T/M712T offspring died at P1-P3 (FIG. 2D). However,
subsequent genotyping of 35 embryos at days E17-E19 showed 26%
Gne.sup.+/+, 43% Gne.sup.M712T/+, and 31% Gne.sup.M712T/M712T,
reflecting a Mendelian distribution, statistically confirmed by
goodness-of-fit testing (|2=0.94, P=0.62) (FIG. 2D). At E17-E19,
the embryos displayed normal exteriors, normal head and body sizes,
and pink skin, which indicated good circulatory and respiratory
function. By P2, however, Gne.sup.M712T/M712T mice were smaller
than control littermates (FIG. 2E), weighing 70%-100% of control
littermates. The Gne.sup.M712T/M712T mouse stomachs contained milk,
although a prominent milkspot was not always visible. All
Gne.sup.M712T/M712T mice except 1 died by P3 and had increased
urinary protein. In contrast, Gne.sup.M712T/+ mice appeared
unaffected.
[0081] Histological analyses. Tissues of Gne.sup.M712T/M712T mice
and their littermates were examined between age P2 and P3. No
abnormalities were identified in skeletal muscle, heart, or liver
(data not shown). Moreover, immunohistochemical staining with
antibodies against laminin and dystrophin failed to show
differences between muscle sections of Gne.sup.M712T/M712T mice and
their wild-type littermates.
[0082] At age P2, kidneys of Gne.sup.M712T/M712T mice showed
petechial hemorrhages by gross examination, but were normal in size
and shape compared with kidneys of Gne.sup.+/+ and Gne.sup.M712T/+
littermates (FIG. 3A). Histological analyses revealed cystic
tubular dilatation (FIG. 3B). High-magnification views of
Gne.sup.M712T/M712T kidneys showed red blood cell infiltrates in
the proximal and distal convoluted tubules and the collecting ducts
(FIG. 3C). The glomeruli of Gne.sup.M712T/M712T mice contained red
blood cell infiltrates in Bowman space (FIG. 3D). Of 100 glomeruli
scored in each group, 64%.+-.6% were affected in
Gne.sup.M712T/M712T mice (n=4) compared with 2%.+-.1% in
Gne.sup.M712T/+ mice (n=3) and 4%.+-.4.5% in Gne.sup.+/+ mice
(n=4). Immunohistochemical analysis demonstrated localization of
Gne/Mnk antibodies to kidney glomeruli (FIG. 3E). Examination of
Gne.sup.M712T/M712T kidneys at E18 showed no histological
differences compared with wild-type or heterozygous littermates
(data not shown).
[0083] Ultrastructural analyses of the glomeruli at age P2 revealed
that, compared with the slender, well-shaped glomerular foot
processes of wild-type mice (FIG. 4A), the podocyte foot process
membranes of Gne.sup.M712T/M712T mice were flattened and largely
fused, with only a few wide foot processes remaining (FIG. 4B).
Filtration slits were reduced in number and showed formation of
tight junction-like structures (FIG. 4B). In addition, the GBM
showed segmental splitting of the lamina densa (FIG. 4B). The size
and shape of endothelial cells lining the basement membrane, as
well as glomerular mesangial cells, appeared ultrastructurally
intact.
[0084] To support these ultrastructural findings, additional
analyses were performed using markers for specific glomerular
compartments. The podocyte-specific markers podocin and podocalyxin
(Pavestadt et al., Physiol. Rev. 83: 253-307 (2003); Dekan et al.
Proc. Natl. Acad. Sci. USA 88: 5398-5402 (1991)) were tested by
immunoblotting kidney extracts of all genotypes. While podocin
showed no difference in expression across all genotypes (at age P1)
(data not shown), podocalyxin, the major sialoglycoprotein of the
podocyte apical membrane (Pavestadt et al.; Dekan et al.),
demonstrated dramatically decreased sialylation (FIG. 6E, upper
gel). Expression levels of GBM markers laminin-1 (FIG. 6C) and
laminin .beta.1 (data not shown) were unchanged in
Gne.sup.M712T/M712T kidneys, as were RNA levels of collagen type IV
.alpha.3 (Col4A3), an integral GBM component. Immunoblotting with
desmin and vascular SMA, antibodies to mesangial cell markers
(Ichimura et al. J. Histochem. Cytochem. 54: 1291-1301 (2006)),
showed similar expression levels across all genotypes. In addition,
real-time quantitative PCR analysis of the endothelial cell marker
CD31/Pecam-1 revealed no difference in RNA expression levels across
genotypes at P1. Serum metabolite studies on the only
Gne.sup.M712T/M712T mouse that survived past weaning demonstrated
elevated blood urea nitrogen levels (39.+-.10 mg/dl in
Gne.sup.M712T/M712T mouse versus 21.+-.2 mg/dl in Gne.sup.+/+ mice)
and increased urinary protein (>500 mg/dl protein), which
indicated renal disease. All other serum metabolites tested,
including creatinine and creatine kinase, were within the normal
ranges. This male Gne.sup.M712T/M712T survivor was euthanized at
age 8.5 months. Histologic analysis revealed no structural
abnormalities in the forelimb or hindlimb. However, severe
bilateral hydronephrosis and changes consistent with glomerulopathy
were found in the kidneys.
[0085] Rescue by ManNAc feeding. ManNAc, added to the drinking
water at a concentration of 1 mg/ml (.about.0.2 g/kg/day) during
matings of Gne.sup.M712T+ mice, yielded no surviving homozygous
Gne.sup.M712T/M712T mice beyond age P3 from among 51 offspring
(FIG. 5A). However, at 5 mg ManNAc/ml (.about.1.0 g/kg/day), among
102 total newborns, 12 Gne.sup.M712T/M712T pups survived beyond P3,
a significantly greater number compared with the 1 survivor in the
untreated group (2-tailed Fisher's exact test, P=0.01) (FIG. 5A).
ManNAc at the administered dose (.about.1.0 g/kg/d) was well
tolerated by the mice, and no side effects were attributed to the
treatment throughout the study. Surviving Gne.sup.M712T/M712T mice
remained smaller than their wild-type littermates, weighing
70%-100%. At age P6, ManNAc treated Gne.sup.M712T/M712T mice
exhibited no abnormalities in liver, heart, or skeletal muscle
tissues (data not shown). Their kidneys demonstrated significant
histological improvement (FIG. 5B-D) compared with
Gne.sup.M712T/M712T mice examined at age P2 (FIG. 3B-D). Upon
ManNAc treatment, there were fewer cystic tubular dilatations in
the cortex and medulla (FIG. 5B) and reduced red blood cell
infiltrates in the tubules and the Bowman space (FIGS. 5C and D).
Ultrastructural analysis at age P19 showed less fusion and
flattening of the podocyte foot processes including a greater
number of open slit diaphragms and an improvement in the "finger
shaping" of the foot processes (FIGS. 4C and D). The overall
integrity of the GBM was also significantly improved, although
occasional segmental splitting of the lamina densa was still
apparent (FIGS. 4C and D).
[0086] The nursing females continued to receive ManNAc treatment
until the pups were weaned (P21). Of the twelve Gne.sup.M712T/M712T
mice that survived past P3, nine died between P6 and P12. One
Gne.sup.M712T/M712T mouse was sacrificed at age P19 for
ultrastructural analysis. Two Gne.sup.M712T/M712T mice survived
past P21, when ManNAc supplementation was ceased. These two mice
continued to grow without receiving additional ManNAc but remained
smaller than their littermates (FIG. 5E). At 3.5 months of age, one
Gne.sup.M712T/M712T survivor was sacrificed because of
hydrocephalus and malocclusion. Similar events occurred in some
untreated mice at different ages and were found not to be related
to treatment or the disease. Skeletal muscle histology of this
mouse revealed no structural or inflammatory abnormalities, but the
kidneys showed mild red blood cell infiltrations in the urinary
space and the tubules. The one surviving Gne.sup.M712T/M712T mouse
is currently 6 months old and has no obvious myopathic
features.
[0087] Biochemical analyses following ManNAc feeding. Gne enzymatic
activity was measured in muscle and kidney at age P2. Skeletal
muscle of Gne.sup.M712T/M712T mice showed 19.4%.+-.7.5 of the Gne
activity of the Gne+/+ mice (n=4, P=0.02) (FIG. 5F). Similar
decreases in Gne activities were measured in Gne.sup.M712T/M712T
kidney extracts (10% of mean Gne.sup.+/+ kidney epimerase
activities). Upon ManNAc treatment, Gne activities in Gne .sup.+/+
muscle (n=3) increased to 114% (.+-.19.7) (P=0.2), while
Gne.sup.M712T/M712T muscle activity (n=7) increased from 19.4%
(.+-.7.5) to 31% (.+-.8.4) of untreated Gne.sup.+/+ mean values of
muscle Gne activity (P=0.05) (FIG. 5F). Immunoblots of muscle and
kidney extracts labeled with anti-Gne/Mnk antibodies demonstrated
38.5% (.+-.27, n=4) Gne/Mnk protein in Gne.sup.M712T/M712T muscle
and 32.1% (.+-.7, n=3) in Gne.sup.M712T/M712T kidney tissues when
compared with Gne.sup.+/+ littermates. This improved upon ManNAc
treatment of Gne.sup.M712T/M712T mice to 68.8% (.+-.20, n=4) in
muscle and to 62.2% (.+-.9.7, n=4) in kidney tissues (P=0.12 and
P=0.006 for muscle and kidney values respectively, relative to
.beta.-actin) (FIGS. 6A and B). Immunoblots stained with antibodies
against laminin-1, an integral component of the GBM (25-27), showed
similar patterns across genotypes before and after treatment (FIG.
6C).
[0088] The degree of sialylation of two heavily sialylated marker
proteins, PSA-NCAM and podocalyxin was evaluated. PSA-NCAM is a
major sialoprotein expressed in neonatal brains (Galuska et al., J.
Biol. Chem. 281: 31605-15 (2006)), where its expression is
regulated by the intracellular concentration of sialic acid (Bork
et al., FEBS letters 579: 5079-83 (2005)).
[0089] FIG. 6 shows that the expression of PSA-NCAM varied within
and between genotypes, yet Gne.sup.M712T/M712T brains at P2 showed
up to 80% decreased PSA-NCAM expression compared with that in
Gne+/+ mice (FIG. 6D, upper gel). A 2%-28% increase compared with
Gne.sup.M712T/M712T untreated mice following ManNAc treatment was
observed (n=14 before treatment and n=10 after treatment, P=0.08)
(FIG. 6D, lower gel). The expression of PSA-NCAM in normal muscle
and kidney at P2 was low, and no change upon treatment in these
tissues could be confirmed (data not shown). In addition, the
significantly decreased sialylation status of podocalyxin in
untreated Gne.sup.M712T/M712T kidneys (FIG. 6E, lower gel) markedly
improved upon ManNAc treatment (FIG. 6E, upper gel).
[0090] Therefore, this Example describes a knockin mice harboring a
M712T Gne/Mnk mutation that was generated by the inventors.
Homozygous mutant (Gne.sup.M712T/M721T) mice did not survive beyond
P3 unless treated with ManNAc. At P2, significantly decreased
Gne-epimerase activity was observed in Gne.sup.M712T/M712T muscle,
but no myopathic features were apparent. Rather, homozygous mutant
mice had glomerular hematuria, proteinuria, and podocytopathy.
Renal findings included segmental splitting of the glomerular
basement membrane, effacement of podocyte foot processes, and
reduced sialylation of the major podocyte sialoprotein,
podocalyxin. ManNAc administration led to survival beyond P3 in 43%
of the Gne.sup.M712T/M712T pups. Survivors exhibited improved renal
histology, increased sialylation of podocalyxin, and increased
Gne/Mnk protein expression and Gne-epimerase activities. These
findings indicate that ManNAc may be a useful treatment not only
for HIBM but also for renal disorders involving proteinuria and
hematuria due to podocytopathy and/or segmental splitting of the
glomerular basement membrane.
EXAMPLE 2
Administration to Humans--Clinical Studies
[0091] Patients will be recruited from the Iranian Jewish
community, from groups of patients known to have HIBM, and from
individuals previously enrolled in protocol 76-HG-0238, "Diagnosis
and Treatment of Patients with Inborn Errors of Metabolism,"
protocol 01-N-0149, "Diagnostic Evaluation of Patients with
Neuromuscular Diseases," or protocol 05-HG-0236, "Pilot Study of
the Use of Intravenous Immune Globulin in Hereditary Inclusion Body
Myopathy." Patients will also be recruited from the patient
organization ARMS (Advancement of Research for Myopathies).
Materials
[0092] ManNAc for human use will be purchased from Meropharm AG
(Eugensbergstrasse 14, 8268 Salenstein, Switzerland). It will be
prepared as 500 mg enteric coated capsules by the Clinical Center
Pharmaceutical Development Service (PDS), who will also prepare a
placebo containing mannose. ManNAc or placebo will be taken orally
in four divided doses, thirty minutes before meals. ManNAc and
placebo capsules will be delivered monthly for each study patient
and stored in the refrigerator. All bottles will be labeled in the
same way and there will be no apparent difference between ManNAc
and placebo capsules in color, shape or taste of the coating.
Procedures
[0093] Baseline evaluations will include a detailed determination
of the extent of neuromuscular disease prior to treatment. The
history and physical examination will include elucidation of the
family pedigree, neurological status, and muscle strength. Baseline
laboratory tests will also include a routine urinalysis. Women will
receive a pregnancy test. Blood will be drawn for CBC and
differential, platelets, erythrocyte sedimentation rate,
electrolytes, calcium, phosphorus, liver enzymes, lipid panel,
alkaline phosphatase, prothrombin time, partial thromboplastin
time, creatine phosphokinase, HbA1C, fasting glucose and insulin,
free T4 and TSH, FSH, LH, testosterone and estradiol. A purple top
tube will be obtained for DNA/RNA extraction, a yellow top for
lymphoblast transformation and separate yellow and brown tops for
platelet and white cell pellets. The DNA/RNA will be used to
perform or confirm mutational analysis of the GNE gene. The cells
will be used for basic research studies, including assessment of
the sialylation status of glycoproteins. Blood and urine will also
be obtained for determination of serum and urine ManNAc and free
sialic acid levels. In addition to spot urine tests, a 24-hour
urine collection will be analyzed for creatinine clearance,
protein, albumin, protein electrophoresis, .beta.2-microglobulin,
and amino acid analysis. Baseline blood tests and their volumes are
as follows:
TABLE-US-00004 Total Volume # Drawn ml/Test (ml) CBC, ESR,
platelets 1 3.0 3.0 Chem 20 panel, CPK, 1 3.5 3.5 & fasting
glucose and lipid panel PT, PTT 1 4.5 4.5 HbA1C, Insulin 1 3.5 3.5
Free T4/TSH 1 3.5 3.5 FSH, LH, Test,, Estradiol 1 5.0 5.0
Lymphoblasts 1 5.0 5.0 Platelet pellet 1 5.0 5.0 Leucocyte
pellet/amino acids 1 5.0 5.0 DNA/RNA 1 8.0 8.0 Serum ManNAc, SA 2
4.0 8.0 Total 54.0
In addition, up to 30 ml of blood may be removed for research
purposes. However, under no circumstances will more than 450 ml of
blood be withdrawn during any 6-week period. Patients' saliva will
also be collected. In addition, a radiograph of the chest, an
echocardiogram and an electrocardiogram and a 24 h ambulatory ECG
will be obtained.
[0094] The primary outcome parameter will be a change in quadriceps
muscle strength, as well as secondary outcome parameters. Maximal
voluntary isometric contraction (MVIC) assessment will be used to
measure changes in the strength of the quadriceps muscles and 10
other muscle groups. MVIC assessment has proven reliable and
sensitive to small changes in the evaluation of myopathy syndromes
and their response to treatment. For MVIC, the quantitative muscle
assessment (QMA) system-version 42+XL will be used. This system
consists of an adjustable strap, attaching the limb to an interface
SM250 force transducer. Patients will be tested on an adjustable
examining table (Neurological Plinth Model), enclosed in a stable
aluminum frame that anchors the transducer. The generated force is
transmitted to an electronic strain-gauge tensiometer and is then
recorded and amplified by the computer-assisted analog/digital data
collection system (S/N A98C36). The measured force is expressed as
the amount of kilograms (kg) that the patient exerts against the
strain gauge.
[0095] Measurements will be performed by standardized testing
modified from the protocol of Andres et al. (Neurology 36, 937-941
(1986)). The following muscle groups will be tested in a fixed
order: right shoulder abductors, right elbow flexors, right elbow
extensors, left shoulder abductors, left elbow flexors, left elbow
extensors, right ankle dorsiflexors, left ankle dorsiflexors, right
knee flexors and left knee flexors, left knee extensors, right knee
extensors. All muscle groups will be tested twice with a minimum of
30 seconds rest between the trials. If measurements differ by more
than 15% a third test will be performed. The average of the two
more similar measurements will be used as the score for that
particular test. The patients will be informed about the test
purpose and procedure before the start of the study and verbal
encouragement will be given during the tests.
[0096] Patients will also perform a 6-minute walk test, a timed
up-and-go test, measures of pinch and grip strength, and the
forward/functional reach test.
[0097] Skeletal muscle strength will also be measured by physical
examination. The 10-point manual muscle testing (MMT-28) scale
(Jain et al. Phys Occup Ther Pediatr 26, 5-17 (2006)), in which 0
is the lowest and 10 the highest score, will be used for grading of
the response. The MMT will be performed by a physical therapist who
will remain blinded and will include physical examination of the
following 13 muscle groups on each side: deltoid, biceps brachii,
triceps brachii, brachioradialis, wrist extensors, wrist flexors,
iliopsoas, gluteus maximus, quadriceps femoris, hamstrings, and
foot extensors and flexors.
[0098] Pulmonary function tests will be performed as a measure of
the strength of the muscles of the thoracic cage. Spirometry, with
or without bronchodilators, will be employed to assess forced vital
capacity (FVC) and forced expiratory volume in 1 sec (FEV1). In
addition, maximal inspiratory and expiratory pressures (MIP and
MEP) and maximum voluntary ventilation (MVV) will be recorded using
standard techniques. The best result of three trials will be
recorded. Lung volumes and diffusion capacity will be assessed at
baseline and repeated if clinically indicated.
[0099] Self-report assessments that capture global clinical
improvement will include the Human Activity Profile (Fix, A. J.,
and Daughton, D. M. (1998) Human Activity Profile Professional
Manual. Psychological Assessment Resources Inc.) and the SF-36v2
quality of life questionnaires (Ware et al. Med Care 30, 473-483
(1992)), to be completed by the patients at the beginning and end
of each crossover period.
[0100] After baseline testing, patients will be randomized and
ManNAc/placebo treatment will begin. The dose will be increased
gradually every two days, as follows: 1 capsule (500 mg)
ManNAc/placebo four times a day (q.i.d.) for two days, followed by
1 capsule q.i.d. incremental increase every two days until the full
dose of .about.10 g, or 5 capsules q.i.d. is reached (FIG. 7).
Serum trough and peak levels (at 30 min, 1, 2 and 4 hours post
administration) of ManNAc, as well as glucose will be obtained
after the first administration of ManNAc on the second day of a
certain dose during the incremental dosing week. At the end of each
treatment period trough and peak (1 hour) levels will be obtained
after each dose over 24 hours.
[0101] Once the full dose of 10 g/day is reached, a repeat ECG or
24 h ambulatory ECG monitoring (Holter), spot urinalysis and the
following blood tests will be performed for safety reasons:
TABLE-US-00005 Total Volume # Drawn ml/Test (ml) CBC, ESR,
platelets 1 3.0 3.0 Chem 20 panel, CPK, 1 3.5 3.5 & fasting
glucose, lipids PT, PTT 1 4.5 4.5 Total 11.0
The patients will be discharged home on the 10 g/day dose, to
return for follow-up admissions at one month and 3 months. This
schedule will be repeated for the second crossover period after a
6-week washout period.
Follow-Up Studies
[0102] Follow-up evaluations will occur at the one-month time point
for each crossover period, and at the end of each crossover period.
They will consist of a one-week admission involving repeat 24-hour
urine studies and the following blood tests:
TABLE-US-00006 Total Volume # Drawn ml/Test (ml) CBC, ESR,
platelets 1 3.0 3.0 Chem 20 panel, CPK, 1 3.5 3.5 & fasting
glucose, lipids PT, PTT 1 4.5 4.5 HbA1C, Insulin 1 3.5 3.5 Free
T4/TSH 1 3.5 3.5 FSH, LH, Test., Estradiol 1 5.0 5.0 Platelet
pellet 1 5.0 5.0 Leucocyte pellet/amino acids 1 5.0 5.0 Serum
ManNAc, SA 1 4.0 8.0 Total 37.0
[0103] Follow-up procedures and consultations will involve repeat
ECG or 24 h ambulatory ECG monitoring (Holter) and echocardiogram,
muscle quantitative strength assessments, functional muscle
studies, PFTs, and functional and quality of life
questionnaires.
[0104] To monitor treatment at home, patients will be asked to
complete a weekly diary (available both electronically and in
hard-copy) in order to record missed doses, GI upset or other
side-effects, and observed improvements.
Statistical Considerations
[0105] Patients will be randomized using a permuted block size to
either ManNAc or placebo (1:1) in a double-blind fashion (block
randomization by the National Institutes of Health Clinical Center
Pharmacy) to ensure balanced assignment to the two groups of
patients with respect to disease duration and severity. There will
be two 3-month crossover periods separated by at least 6-week
washout period. Each patient will serve as his/her own control. The
randomization code will not be broken until completion of the study
and analysis of the results.
[0106] The primary clinical outcome parameter will be change in
quadriceps muscle strength, assessed by maximum voluntary isometric
contraction testing (MVIC) that will be performed at baseline, 1
month after initiation of treatment and at the end of each
treatment period. Change in strength (kg) will be expressed as % of
baseline. Paired t-tests and the Wilcoxon matched pairs signed rank
test will be employed for the analysis.
[0107] Secondary outcome parameters will include functional muscle
testing using the 6-minute walk test, functional reach, timed
up-and-go, grip strength and pulmonary function tests. Lastly, each
patient's global assessment of improvement will be based on the
Human Activity Profile (ALSFRS) and SF-36 quality of life
questionnaires, and specific self-assessment scores will be
obtained for depression, fatigue, and function.
[0108] The estimated sample size is based upon different pieces of
data, including the inventors' experience with four HIBM patients
whose muscle strength was quantified before and after a month of
intravenous immune globulin treatments as a source of sialic acid
(Sparks, S., et al. BMC Neurol 7, 3 (2007)). There was a highly
significant correlation between the change in left quadriceps
strength and the change in right quadriceps strength. Therefore,
the mean of the two sides as the primary outcome parameter will be
used in larger clinical studies. Next, a change of 0% in patients
before and after the 3-month placebo treatment will be assumed,
based upon the fact that significant progression of muscle weakness
takes years to occur. An estimated 10% standard deviation is
expected for the baseline and post-treatment measurements, and a
10% standard deviation for the mean difference, which would be 0
for placebo treatment. The coefficient of variation for the MIVC
method of quantitative muscle strength testing in the literature is
6-15%. Andres, P. L., et al. Neurology 36, 937-941 (1986); Colombo,
R., et al. Med Eng Phys 22, 167-174 (2000); A comparison of muscle
strength testing techniques in amyotrophic lateral sclerosis.
Neurology 61, 1503-1507 (2003); Mayhew, J. E., et al. Muscle Nerve
35, 36-42 (2007); Symons, T. B., et al. J Gerontol A Biol Sci Med
Sci 60, 114-11 (2005).
[0109] A 20% improvement in quadriceps muscle strength is
predicted, based upon several considerations. First, this would be
a clinically significant improvement, and a smaller benefit might
not detectable or significant. Second, in intravenous immune
globulin (IVIG) study conducted by the inventors, the mean (SD)
improvement in strength for the 8 quadriceps of 4 treated patients
was 39.+-.50%, so that a 20% improvement is conservative. Third,
assuming complete absorption and conversion of ManNAc to sialic
acid, 1000 times the sialic acid is delivered compared to the
amount of IVIG delivered in the previous study. A standard
deviation of muscle strength change under ManNAc treatment is
estimated to be 26%, because the SD/mean ratio of 26/20 is the same
as the SD/mean ratio of 50/39 observed in the IVIG study.
[0110] Under these conditions, a 20% difference will be detected
using 18 patients with a power of 0.90 and p=0.05. Twenty patients
will be treated, with the expectation that two to drop out. Up to
30 patients will hopefully be enrolled to obtain 20 who meet
eligibility requirements.
[0111] This power analysis is conservative, since one-month data
could strengthen the effect, a 20% improvement may be an
underestimate, and the relative SD for % improvement of 18 patients
is likely to be less than that of the 4 patients upon whom we based
the estimate. Changes in secondary outcome parameters will be
analyzed using a one-tailed t-test and p=0.025.
[0112] Oral ManNAc supplementation could provide HIBM patients with
transient improvements in muscle strength and feelings of
well-being. It may also prevent deterioration in their clinical
course and be useful in treating the muscle weakness of HIBM. The
clinical trial will also establish the safety and tolerability of
ManNAc for human use. This may serve as a basis for other potential
therapeutic applications of ManNAc, such as the potential benefit
for podocytopathies and glomerular basemement membrane diseases
suggested from our animal studies.
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[0180] All patents and publications referenced or mentioned herein
are indicative of the levels of skill of those skilled in the art
to which the invention pertains, and each such referenced patent or
publication is hereby incorporated by reference to the same extent
as if it had been incorporated by reference in its entirety
individually or set forth herein in its entirety. Applicants
reserve the right to physically incorporate into this specification
any and all materials and information from any such cited patents
or publications.
[0181] The specific methods and compositions described herein are
representative of preferred embodiments and are exemplary and not
intended as limitations on the scope of the invention. Other
objects, aspects, and embodiments will occur to those skilled in
the art upon consideration of this specification, and are
encompassed within the spirit of the invention as defined by the
scope of the claims. It will be readily apparent to one skilled in
the art that varying substitutions and modifications may be made to
the invention disclosed herein without departing from the scope and
spirit of the invention. The invention illustratively described
herein suitably may be practiced in the absence of any element or
elements, or limitation or limitations, which is not specifically
disclosed herein as essential. The methods and processes
illustratively described herein suitably may be practiced in
differing orders of steps, and that they are not necessarily
restricted to the orders of steps indicated herein or in the
claims. As used herein and in the appended claims, the singular
forms "a," "an," and "the" include plural reference unless the
context clearly dictates otherwise. Thus, for example, a reference
to "an antibody" includes a plurality (for example, a solution of
antibodies or a series of antibody preparations) of such
antibodies, and so forth. Under no circumstances may the patent be
interpreted to be limited to the specific examples or embodiments
or methods specifically disclosed herein. Under no circumstances
may the patent be interpreted to be limited by any statement made
by any Examiner or any other official or employee of the Patent and
Trademark Office unless such statement is specifically and without
qualification or reservation expressly adopted in a responsive
writing by Applicants.
[0182] The terms and expressions that have been employed are used
as terms of description and not of limitation, and there is no
intent in the use of such terms and expressions to exclude any
equivalent of the features shown and described or portions thereof,
but it is recognized that various modifications are possible within
the scope of the invention as claimed. Thus, it will be understood
that although the present invention has been specifically disclosed
by preferred embodiments and optional features, modification and
variation of the concepts herein disclosed may be resorted to by
those skilled in the art, and that such modifications and
variations are considered to be within the scope of this invention
as defined by the appended claims.
[0183] The invention has been described broadly and generically
herein. Each of the narrower species and subgeneric groupings
falling within the generic disclosure also form part of the
invention. This includes the generic description of the invention
with a proviso or negative limitation removing any subject matter
from the genus, regardless of whether or not the excised material
is specifically recited herein.
[0184] Other embodiments are within the following claims. In
addition, where features or aspects of the invention are described
in terms of Markush groups, those skilled in the art will recognize
that the invention is also thereby described in terms of any
individual member or subgroup of members of the Markush group.
Sequence CWU 1
1
81722PRTMus musculus 1Met Glu Lys Asn Gly Asn Asn Arg Lys Leu Arg
Val Cys Val Ala Thr1 5 10 15 Cys Asn Arg Ala Asp Tyr Ser Lys Leu
Ala Pro Ile Met Phe Gly Ile 20 25 30 Lys Thr Glu Pro Ala Phe Phe
Glu Leu Asp Val Val Val Leu Gly Ser 35 40 45 His Leu Ile Asp Asp
Tyr Gly Asn Thr Tyr Arg Met Ile Glu Gln Asp 50 55 60 Asp Phe Asp
Ile Asn Thr Arg Leu His Thr Ile Val Arg Gly Glu Asp65 70 75 80 Glu
Ala Ala Met Val Glu Ser Val Gly Leu Ala Leu Val Lys Leu Pro 85 90
95 Asp Val Leu Asn Arg Leu Lys Pro Asp Ile Met Ile Val His Gly Asp
100 105 110 Arg Phe Asp Ala Leu Ala Leu Ala Thr Ser Ala Ala Leu Met
Asn Ile 115 120 125 Arg Ile Leu His Ile Glu Gly Gly Glu Val Ser Gly
Thr Ile Asp Asp 130 135 140 Ser Ile Arg His Ala Ile Thr Lys Leu Ala
His Tyr His Val Cys Cys145 150 155 160 Thr Arg Ser Ala Glu Gln His
Leu Ile Ser Met Cys Glu Asp His Asp 165 170 175 Arg Ile Leu Leu Ala
Gly Cys Pro Ser Tyr Asp Lys Leu Leu Ser Ala 180 185 190 Lys Asn Lys
Asp Tyr Met Ser Ile Ile Arg Met Trp Leu Gly Asp Asp 195 200 205 Val
Lys Cys Lys Asp Tyr Ile Val Ala Leu Gln His Pro Val Thr Thr 210 215
220 Asp Ile Lys His Ser Ile Lys Met Phe Glu Leu Thr Leu Asp Ala
Leu225 230 235 240 Ile Ser Phe Asn Lys Arg Thr Leu Val Leu Phe Pro
Asn Ile Asp Ala 245 250 255 Gly Ser Lys Glu Met Val Arg Val Met Arg
Lys Lys Gly Ile Glu His 260 265 270 His Pro Asn Phe Arg Ala Val Lys
His Val Pro Phe Asp Gln Phe Ile 275 280 285 Gln Leu Val Ala His Ala
Gly Cys Met Ile Gly Asn Ser Ser Cys Gly 290 295 300 Val Arg Glu Val
Gly Ala Phe Gly Thr Pro Val Ile Asn Leu Gly Thr305 310 315 320 Arg
Gln Ile Gly Arg Glu Thr Gly Glu Asn Val Leu His Val Arg Asp 325 330
335 Ala Asp Thr Gln Asp Lys Ile Leu Gln Ala Leu His Leu Gln Phe Gly
340 345 350 Lys Gln Tyr Pro Cys Ser Lys Ile Tyr Gly Asp Gly Asn Ala
Val Pro 355 360 365 Arg Ile Leu Lys Phe Leu Lys Ser Ile Asp Leu Gln
Glu Pro Leu Gln 370 375 380 Lys Lys Phe Cys Phe Pro Pro Val Lys Glu
Asn Ile Ser Gln Asp Ile385 390 395 400 Asp His Ile Leu Glu Thr Leu
Ser Ala Leu Ala Val Asp Leu Gly Gly 405 410 415 Thr Asn Leu Arg Val
Ala Ile Val Ser Met Lys Gly Glu Ile Val Lys 420 425 430 Lys Tyr Thr
Gln Phe Asn Pro Lys Thr Tyr Glu Glu Arg Ile Ser Leu 435 440 445 Ile
Leu Gln Met Cys Val Glu Ala Ala Ala Glu Ala Val Lys Leu Asn 450 455
460 Cys Arg Ile Leu Gly Val Gly Ile Ser Thr Gly Gly Arg Val Asn
Pro465 470 475 480 Gln Glu Gly Val Val Leu His Ser Thr Lys Leu Ile
Gln Glu Trp Asn 485 490 495 Ser Val Asp Leu Arg Thr Pro Leu Ser Asp
Thr Leu His Leu Pro Val 500 505 510 Trp Val Asp Asn Asp Gly Asn Cys
Ala Ala Met Ala Glu Arg Lys Phe 515 520 525 Gly Gln Gly Lys Gly Gln
Glu Asn Phe Val Thr Leu Ile Thr Gly Thr 530 535 540 Gly Ile Gly Gly
Gly Ile Ile His Gln His Glu Leu Ile His Gly Ser545 550 555 560 Ser
Phe Cys Ala Ala Glu Leu Gly His Leu Val Val Ser Leu Asp Gly 565 570
575 Pro Asp Cys Ser Cys Gly Ser His Gly Cys Ile Glu Ala Tyr Ala Ser
580 585 590 Gly Met Ala Leu Gln Arg Glu Ala Lys Lys Leu His Asp Glu
Asp Leu 595 600 605 Leu Leu Val Glu Gly Met Ser Val Pro Lys Asp Glu
Ala Val Gly Ala 610 615 620 Leu His Leu Ile Gln Ala Ala Lys Leu Gly
Asn Val Lys Ala Gln Ser625 630 635 640 Ile Leu Arg Thr Ala Gly Thr
Ala Leu Gly Leu Gly Val Val Asn Ile 645 650 655 Leu His Thr Met Asn
Pro Ser Leu Val Ile Leu Ser Gly Val Leu Ala 660 665 670 Ser His Tyr
Ile His Ile Val Lys Asp Val Ile Arg Gln Gln Ala Leu 675 680 685 Ser
Ser Val Gln Asp Val Asp Val Val Val Ser Asp Leu Val Asp Pro 690 695
700 Ala Leu Leu Gly Ala Ala Ser Met Val Leu Asp Tyr Thr Thr Arg
Arg705 710 715 720 Ile His2722PRTArtificial SequenceA synthetic
polypeptide 2Met Glu Lys Asn Gly Asn Asn Arg Lys Leu Arg Val Cys
Val Ala Thr1 5 10 15 Cys Asn Arg Ala Asp Tyr Ser Lys Leu Ala Pro
Ile Met Phe Gly Ile 20 25 30 Lys Thr Glu Pro Ala Phe Phe Glu Leu
Asp Val Val Val Leu Gly Ser 35 40 45 His Leu Ile Asp Asp Tyr Gly
Asn Thr Tyr Arg Met Ile Glu Gln Asp 50 55 60 Asp Phe Asp Ile Asn
Thr Arg Leu His Thr Ile Val Arg Gly Glu Asp65 70 75 80 Glu Ala Ala
Met Val Glu Ser Val Gly Leu Ala Leu Val Lys Leu Pro 85 90 95 Asp
Val Leu Asn Arg Leu Lys Pro Asp Ile Met Ile Val His Gly Asp 100 105
110 Arg Phe Asp Ala Leu Ala Leu Ala Thr Ser Ala Ala Leu Met Asn Ile
115 120 125 Arg Ile Leu His Ile Glu Gly Gly Glu Val Ser Gly Thr Ile
Asp Asp 130 135 140 Ser Ile Arg His Ala Ile Thr Lys Leu Ala His Tyr
His Val Cys Cys145 150 155 160 Thr Arg Ser Ala Glu Gln His Leu Ile
Ser Met Cys Glu Asp His Asp 165 170 175 Arg Ile Leu Leu Ala Gly Cys
Pro Ser Tyr Asp Lys Leu Leu Ser Ala 180 185 190 Lys Asn Lys Asp Tyr
Met Ser Ile Ile Arg Met Trp Leu Gly Asp Asp 195 200 205 Val Lys Cys
Lys Asp Tyr Ile Val Ala Leu Gln His Pro Val Thr Thr 210 215 220 Asp
Ile Lys His Ser Ile Lys Met Phe Glu Leu Thr Leu Asp Ala Leu225 230
235 240 Ile Ser Phe Asn Lys Arg Thr Leu Val Leu Phe Pro Asn Ile Asp
Ala 245 250 255 Gly Ser Lys Glu Met Val Arg Val Met Arg Lys Lys Gly
Ile Glu His 260 265 270 His Pro Asn Phe Arg Ala Val Lys His Val Pro
Phe Asp Gln Phe Ile 275 280 285 Gln Leu Val Ala His Ala Gly Cys Met
Ile Gly Asn Ser Ser Cys Gly 290 295 300 Val Arg Glu Val Gly Ala Phe
Gly Thr Pro Val Ile Asn Leu Gly Thr305 310 315 320 Arg Gln Ile Gly
Arg Glu Thr Gly Glu Asn Val Leu His Val Arg Asp 325 330 335 Ala Asp
Thr Gln Asp Lys Ile Leu Gln Ala Leu His Leu Gln Phe Gly 340 345 350
Lys Gln Tyr Pro Cys Ser Lys Ile Tyr Gly Asp Gly Asn Ala Val Pro 355
360 365 Arg Ile Leu Lys Phe Leu Lys Ser Ile Asp Leu Gln Glu Pro Leu
Gln 370 375 380 Lys Lys Phe Cys Phe Pro Pro Val Lys Glu Asn Ile Ser
Gln Asp Ile385 390 395 400 Asp His Ile Leu Glu Thr Leu Ser Ala Leu
Ala Val Asp Leu Gly Gly 405 410 415 Thr Asn Leu Arg Val Ala Ile Val
Ser Met Lys Gly Glu Ile Val Lys 420 425 430 Lys Tyr Thr Gln Phe Asn
Pro Lys Thr Tyr Glu Glu Arg Ile Ser Leu 435 440 445 Ile Leu Gln Met
Cys Val Glu Ala Ala Ala Glu Ala Val Lys Leu Asn 450 455 460 Cys Arg
Ile Leu Gly Val Gly Ile Ser Thr Gly Gly Arg Val Asn Pro465 470 475
480 Gln Glu Gly Val Val Leu His Ser Thr Lys Leu Ile Gln Glu Trp Asn
485 490 495 Ser Val Asp Leu Arg Thr Pro Leu Ser Asp Thr Leu His Leu
Pro Val 500 505 510 Trp Val Asp Asn Asp Gly Asn Cys Ala Ala Met Ala
Glu Arg Lys Phe 515 520 525 Gly Gln Gly Lys Gly Gln Glu Asn Phe Val
Thr Leu Ile Thr Gly Thr 530 535 540 Gly Ile Gly Gly Gly Ile Ile His
Gln His Glu Leu Ile His Gly Ser545 550 555 560 Ser Phe Cys Ala Ala
Glu Leu Gly His Leu Val Val Ser Leu Asp Gly 565 570 575 Pro Asp Cys
Ser Cys Gly Ser His Gly Cys Ile Glu Ala Tyr Ala Ser 580 585 590 Gly
Met Ala Leu Gln Arg Glu Ala Lys Lys Leu His Asp Glu Asp Leu 595 600
605 Leu Leu Val Glu Gly Met Ser Val Pro Lys Asp Glu Ala Val Gly Ala
610 615 620 Leu His Leu Ile Gln Ala Ala Lys Leu Gly Asn Val Lys Ala
Gln Ser625 630 635 640 Ile Leu Arg Thr Ala Gly Thr Ala Leu Gly Leu
Gly Val Val Asn Ile 645 650 655 Leu His Thr Met Asn Pro Ser Leu Val
Ile Leu Ser Gly Val Leu Ala 660 665 670 Ser His Tyr Ile His Ile Val
Lys Asp Val Ile Arg Gln Gln Ala Leu 675 680 685 Ser Ser Val Gln Asp
Val Asp Val Val Val Ser Asp Leu Val Asp Pro 690 695 700 Ala Leu Leu
Gly Ala Ala Ser Thr Val Leu Asp Tyr Thr Thr Arg Arg705 710 715 720
Ile His32654DNAMus musculus 3gctaaaccag aggccagacg gcagctcagg
agtccgacca cacctcagga aacagctgtg 60ccacaggatg gaaacacacg cgcatctcca
cagggagcag agctacgcag gacctcatga 120actctatttt aagaaactct
caagtaaaaa gaagcaagtc atggagaaga acgggaacaa 180ccgaaagctc
cgggtttgcg ttgccacctg caaccgagct gactactcca aactggcccc
240gatcatgttc ggcatcaaga cagagcccgc gttctttgag ttggacgtgg
tggtgctcgg 300ctcccacctg attgacgact atggaaacac ataccgcatg
attgagcaag atgactttga 360cattaacacc aggctccaca cgattgttag
aggggaagat gaagcggcca tggtagagtc 420ggtaggccta gcgctcgtga
agctaccgga cgtcctcaat cgcctgaagc ccgacatcat 480gattgttcac
ggagaccgat ttgacgccct tgctctggct acgtctgctg ccttgatgaa
540catccgcatc cttcacattg aaggaggcga ggtcagcggg accattgatg
actctatcag 600acacgccata acaaaactgg ctcactacca tgtgtgctgc
actagaagtg cagagcagca 660cctgatctct atgtgcgagg accacgaccg
catcctgttg gcaggctgcc cttcctatga 720caaactgctc tccgccaaga
acaaagacta tatgagcatc attcggatgt ggctaggcga 780tgatgtaaaa
tgtaaggatt acatcgttgc cctgcagcat cccgtgacca ctgacattaa
840gcattccata aagatgtttg agctaacact ggatgccctg atctcgttta
acaagaggac 900cctagttctg tttccaaata tcgatgcagg cagcaaggag
atggttcgag tgatgcggaa 960gaagggcatc gagcatcacc ccaatttccg
tgcagtcaag cacgtcccgt ttgaccagtt 1020catacagctg gtcgcccacg
ctggctgcat gattgggaat agcagctgcg gcgtgcgaga 1080ggttggcgct
ttcggaacac ccgtgatcaa cctgggcaca aggcagatag gaagagaaac
1140cggggagaat gttcttcatg tcagggatgc tgacacccaa gataaaatat
tgcaagcact 1200acacctccag ttcggcaaac agtacccttg ctcaaagata
tatggggatg ggaatgctgt 1260tccaaggatt ttaaagtttc tcaaatccat
tgaccttcaa gagccactac agaagaaatt 1320ctgcttcccc cctgtaaagg
agaacatctc tcaagacatt gaccacatcc tggaaactct 1380gagtgccttg
gctgttgatc ttggcgggac aaacctgagg gtggcaatag ttagcatgaa
1440gggtgaaatc gttaagaagt acactcagtt caaccctaaa acctatgaag
aaaggattag 1500tttaatcctg cagatgtgtg tggaagctgc cgcggaagct
gtgaaactca attgcagaat 1560tctgggagta ggcatctcca caggtggccg
cgtgaatccc caggaaggag ttgtgctgca 1620ttcaaccaag ctgatccagg
aatggaactc cgtggacctc aggacacccc tctccgacac 1680cctgcatctc
cccgtgtggg tggacaatga cggcaactgt gccgccatgg cagagaggaa
1740gttcggccaa ggaaaaggac aggagaactt cgtgacgctc atcacgggga
cagggatcgg 1800tggggggatc atccaccagc acgaactgat ccacggcagc
tccttctgcg cggcggagct 1860cggccatctc gtggtgtccc tggacggtcc
tgactgctcc tgtggaagcc atgggtgcat 1920cgaagcgtac gcctctggaa
tggccttgca gagggaagca aagaaactcc atgatgagga 1980cctgctcttg
gtggaaggga tgtcagtacc aaaagacgaa gctgtgggtg ccctccatct
2040catccaggct gccaagctgg gcaacgtgaa ggcccagagc atcttacgaa
cagctggaac 2100tgctttggga cttggggttg tgaacatcct ccacactatg
aatccttccc tggtgatcct 2160gtctggagtc ctggccagtc actacatcca
catcgtgaag gacgtcatcc gccagcaagc 2220cttgtcctcc gtgcaggatg
tggacgtggt ggtctcagac ttggtggacc cggccctgct 2280tggcgcagcc
agcatggttc tggactacac aacgcgcagg atccactagg tctcccggga
2340acggacacgg acagagactc gggagctgct tagagtggaa ccatgctctt
ctagatcagt 2400gtttctgcga aggcaaattt ggggggaggg ctgctgagac
agctcagtgg ttaagagcct 2460gccctgctcc tgccagtccc cagcacccat
gtcaggcagc tcagctgcct ggaagccaag 2520ctccagggga cccaatgcct
ctctgccggg ggcagctgca ctcagatgta catacccctc 2580tccacacaca
tacaaataaa gcttattttt caaaaggcaa aaaaaaaaaa aaaaaaaaaa
2640aaaaaaaaaa aaaa 2654420DNAArtificial SequenceA synthetic
oligonucleotide 4agcacttcct gagtttgatg 20522DNAArtificial SequenceA
synthetic oligonucleotide 5atttgccttc gcagacactt ga
22620DNAArtificial SequenceA synthetic oligonucleotide 6gcccagagca
tcttacgaac 20718PRTArtificial SequenceA synthetic oligonucleotide
7Gly Gly Gly Thr Cys Cys Cys Cys Thr Gly Gly Ala Gly Cys Thr Thr1 5
10 15 Gly Gly820PRTMus musculus 8Glu Ala Tyr Ala Ser Gly Met Ala
Leu Gln Arg Glu Ala Lys Lys Leu1 5 10 15 His Asp Glu Asp 20
* * * * *